Sandra Finley

Sep 102009
 

Canada’s GM contaminated flax has now been found in 28 countries

CONTENTS

(1)    “TRIFFID” GM FLAX COMING TO YOU, COMPLIMENTS OF THE UNIVERSITY?

(2)   TRIFFID ENGINEERED TO BE RESISTANT TO CHEMICAL RESIDUE IN SOIL

(3)   CANADIAN FOOD INSPECTION AGENCY (CFIA) IS RESPONIBLE FOR LICENSING CROPS.  IT CONTINUES TO SHOW TRIFFID AUTHORIZED FOR “UNCONFINED RELEASE”.

(4)   NEWS REPORTS, GM CONTAMINATION OF CANADIAN FLAX EXPORTS THREATEN MARKETS IN EUROPE

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

(1)    “TRIFFID” GM FLAX COMING TO YOU, COMPLIMENTS OF THE UNIVERSITY?

Triffid flax is GM and came out of the CDC (the Crop Development Centre) at the University of Saskatchewan.

Ten years ago Terry Boehm was a critical player in the Flax Council’s success in preventing the introduction of GM flax into Canada.  Farmers knew they would lose international flax markets if Canadian flax became contaminated with GM seeds.  They had experience with GM canola.

The following is consistent with what I’ve read and heard:  http://www.spinprofiles.org/index.php/Alan_McHughen

“ … on September 10, 2009 the European Union (EU) Rapid Alert System for Food and Feed (RASFF) reported finding an unapproved genetically modified (GM) flax/linseed variety in cereal and bakery products in Germany. The Canadian flax seed market promptly collapsed. The brand name of this GM flax was Triffid, and it was developed and registered for use in Canada by Alan McHughen.

McHughen’s seed

Alan McHughen, over the strong and vigorous objections of the flax growers in Canada, insisted on bioengineering and then registering the GM Triffid flax with public funds through the University of Saskatchewan Crop Development Center.[5] Triffid was approved by Canadian regulators in 1998 but the Flax Council of Canada convinced the Canadian Food Inspection Agency to remove variety registration for the GM flax in 2001, making it illegal to grow.  

(INSERT:  I don’t understand. See Item #3 – the CFIA still shows Triffid as “authorized”. )

 Flax growers took this action to protect their export markets from the threat of GM contamination.[6] The University of Saskatchewan lost a substantial sum of money from this episode.[7][8][9]  

(INSERT:  it has been reported that the development costs alone ran to over $2 million dollars.)

In September 2009 Resource News International reported:

Cash bids for flaxseed in Western Canada have taken a dramatic turn for the worse with some of the decline being linked to European concerns the crop contains genetically modified organisms (GMOs).

GM flax FP967 (CDC Triffid) has tolerance to soil residues of sulfonylurea-based herbicides. Canada supplies approximately 70% of the total flax/linseed utilized in the EU annually.[11]

An article by Allan Dawson in the Manitoba Co-operator (“CDC Triffid Flax Scare Threatens Access To No. 1 EU Market”, September 17 2009), states that McHughen deliberately spread his GM Triffid flax seed by giving away packets to farmers to plant, at a time when the flax industry was trying to eradicate the GM threat from its crop:

Alan McHughen, who developed CDC Triffid, gave away small packets of the seed early in the decade — a move criticized by the flax industry at the time.[12]  

(INSERT:  I talked with Percy Schmeiser.  He said that McHughen also gave out packets of 144 seeds each, to rural school students to take home.  But I wonder how vigilant was the collection of the Triffid seed when it was all to have been destroyed ?  The University had sold the seed.)  . . .

Testing did confirm that the contaminant was Triffid. In January 2010, an article for CBC News reported:

Canadian flax seed has been shut out of its largest market after traces of Triffid — a genetically modified form of the crop ordered destroyed 10 years ago — was found in shipments. The European Union, which buys 70 per cent of Canada’s flax, has a zero-tolerance policy regarding genetically modified organisms and has been turning away shipments. … “

Officials say Canada’s entire $320-million industry is threatened.[14]  . . .

So what happened?  . . . OOPS!  Somehow GM flax sneaked its way out.  And OOPS!  The Europeans discovered it in their shipments of flax from Canada in September 2009.  And OOPS!  They turned it back.  And OOPS!  We’re talking about flax, worth $320 million dollars in sales, not to mention the other costs associated with it.

Lame excuses:

–          “ …  managing director (of the CDC) Dorothy Murrell told CBC News.  “We’re puzzled, but regardless of that, we’re taking action and trying to do our part . . “

–        “ …  The modified seed was deregistered and ordered destroyed 10 years ago . . .   Mysteriously, Triffid has reappeared in commercial crops.”

Where is our backbone?  We are talking about our food supply.

NOT ONLY THAT:

–        if Canadian farmers sue over the loss of flax markets (as the American farmers sued over loss of rice markets), the case will be against the University.   WE are the ones who will pay … again, and in several ways.

The University Administration needs to be held accountable.  There is no accountability if very few people know about the situation.

= = = = = = = ==

(2)   TRIFFID ENGINEERED TO BE RESISTANT TO CHEMICAL RESIDUE IN SOIL

Science and universities. . . .   The Canadian Food Inspection Agency (CFIA – Dept of Agriculture) says this about the University’s Triffid flax:

“This plant was transformed with genes conferring tolerance to soil residues of the herbicides triasulfuron and metsulfuron- methyl . . “.  (http://www.inspection.gc.ca/english/plaveg/bio/dd/dd9824e.shtml )

Do I read correctly?  Is this about:

–        Problem:  a gradual build-up in chemical contamination of the soil has negative impact on plant growth

–        Response:  genetically-manipulate the food crop so it can grow in spite of the residues of the chemicals in the soil.

?  Do I misunderstand?  Because if I understand correctly, this seems to me to be a colossally stupid response to the problem.  I must be wrong.

But then, in recent news over the melting of the Polar Ice Cap the scientists once again stress the chemicals found in the ice samples.  Expect the University to connect the dots?  Chemical agriculture – – maybe we should be finding different ways of crop production?  Deny there is any relationship between the work at the University on chemical and biotech agriculture and the known problems they are creating?

Truth-seekers?  Propaganda that passes for education?  The “product” they sell to their “consumers” (students)?  The University as a place for helping to find answers to the society’s problems?

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

(3)  CANADIAN FOOD INSPECTION AGENCY (CFIA) IS RESPONIBLE FOR LICENSING CROPS.  IT SHOWS TRIFFID AUTHORIZED FOR “UNCONFINED RELEASE”.

Today (2010), if you read the “Decision Document” for Triffid, the Canadian Food Inspection Agency (Agriculture Canada), responsible for licensing says “Unconfined release into the environment and livestock feed use of CDC Triffid is therefore authorized.”

http://www.inspection.gc.ca/english/plaveg/bio/dd/dd9824e.shtml )

1996-05.   Last date modified: 2001-07-18”

(Note:  CDC = Crop Development Centre)

I don’t understand:  Triffid GM flax was supposed to have been made illegal in 2001 ??

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

(4)  NEWS REPORTS, GM CONTAMINATION OF CANADIAN FLAX EXPORTS THREATEN MARKETS IN EUROPE (for a quick scroll-through)

GM contamination of Canadian flax exports threatens markets in Europe

Posted by National Farmers Union on Sept/10/09

The European Commission’s Rapid Alert System for Food and Feed has confirmed the contamination of Canadian flax exports with a genetically modified (GM) flax, devastating Canadian flax sales to Europe. The GM flax has been illegal to grow in Canada since 2001 when flax growers forced the government to take the product off the market. A German company confirmed the GM contamination in its cereals and bakery products.

The GM flax, called the “Triffid”, was approved by Canadian regulators in 1998 but the Flax Council of Canada convinced the Canadian Food Inspection Agency to remove variety registration for the GM flax in 2001, making it illegal to grow. Flax growers took this action to protect their export markets from the threat of GM contamination. Approximately 70 per cent of Canada’s flax is exported to Europe.

“This is an absolute nightmare for flax growers and why we worked so hard to have the GM flax removed,” said Terry Boehm, a flax grower and Vice President of the National Farmers Union. “Flax growers forced the GM flax off the market eight years ago to prevent any threat of contamination and protect our export markets. GM flax was never wanted or needed. We knew it would destroy our European markets and now we fear this has happened.”

At the beginning of this month, cash bids for flaxseed in Western Canada fell dramatically based on rumours of GM contamination.

“This contamination is extremely shocking as GM flax has not been grown in Canada since 2001,” said Lucy Sharratt, Coordinator of the Canadian Biotechnology Action Network. “Where did this contamination come from?”

“This is a major international contamination incident that shows how dangerous any GM crop field testing and development is for farmers and consumers,” said Arnold Taylor, an organic flax grower and Chair of the Organic Agriculture Protection Fund of the Saskatchewan Organic Directorate.

“Germany never approved GM flax but thanks to Canada we are eating illegal and unlicensed flax in our bread and cereal,” said Stefanie Hundsdorfer from Greenpeace Germany. “This again proves that once released into nature genetically engineered constructs are uncontrollable and cannot be recalled. At least now it’s clear that the industry is unable to control its products.”

The GM flax was developed by controversial scientist and industry proponent Alan McHughen when he worked at the Crop Development Centre of the University of Saskatchewan. In the wake of the 2001 controversy the Centre halted its GM research.

This revelation of GM flax contamination comes right in the middle of another huge scandal over Canada’s approval of Monsanto’s eight-trait GE ‘SmartStax’ corn without any health safety assessment.

“Consumers are reeling from learning that Health Canada did not approve the new ‘SmartStax’ GM corn and now they find out that their flax could be contaminated,” said Sharratt. “GM is out of control, we clearly need a moratorium on all new GM crops and foods until we can examine the entire system that regulates GM in Canada. . . . – – – – – – – – – – – – – – – —

(Link no longer valid http://www.gmcontaminationregister.org/index.php?content=nw_detail1)

“Since that first discovery (Sept 08, 2009) GM flax continues to be discovered around Europe and is thought to have been imported to over 30 countries around the world. The table at the bottom of the page shows confirmed cases… “

– – – – – – – – – – – – – – – —

http://www.searice.org.ph/

GM Flax Seed Yanked Off Canadian

Market – Rounded Up, Crushed

By Jason Warick

The StarPhoenix

http://www.thestarphoenix.com/

2006-23-1

A genetically modified (GM) flax seed developed at the University of Saskatchewan has been taken off the market because of European fears the variety will contaminate other flax produced in Canada.

The last of the 200,000 bushels of Triffid flax seed worth at least $2.5 million was rounded up from farms across the Prairies and crushed earlier this year and deregistered April 1.

“Yes, it was frustrating. We lost money. We lost a chance to provide a useful product to our customers,” said John Allen, director of market development for Quality Assured Seeds, a farmer-owned company that was licensed by the U of S to sell Triffid.

Triffid, named after the tall, three-legged walking plants in a 1950s science fiction novel and movie, is now illegal to sell or grow in Canada.

Crop varieties are commonly deregistered when they become obsolete or defects are discovered. The Triffid case is unique because it’s the first time a productive, federally approved crop has been removed from the market.

It’s also the first time farmers have led the call to make a crop unavailable to them.

Triffid, modified to be resistant to the herbicide sulfonylurea, was developed by U of S Crop Development Centre senior research scientist Alan McHughen and registered with the Canadian Food Inspection Agency in the mid-1990s.

The licence was granted to the Regina company, and Allen said they “anticipated a substantial amount of profit” from the sales. The U of S also stood to profit from the royalties.

But European customers, which buy 60 per cent of Canada’s flax, said they didn’t want to buy any GM flax.

Canadian flax farmers and producer groups, afraid the Europeans would label all Canadian flax as contaminated, pushed for the elimination of Triffid.

“We acted as the catalyst. We got the production shut down,” said Barry Hall, president of the Flax Council of Canada.

“It was one more step to reassure our European customers.”

The Saskatchewan Flax Development Commission also pushed for deregistration. “We’re concerned about losing markets. European customers are not interested in GM flax. We felt we should address the issue,” said commission executive director.

The seed was never grown commercially, but roughly 40 farmers from across the Prairies were multiplying the 200,000 bushels of seed for future marketing and use.

They had to clean out their flax bins and ship the seed to Canamera Foods in Manitoba for crushing.

Once the food inspection agency had written assurances all of Canada’s Triffid seed had been eliminated, the variety was deregistered this spring.

“There was nothing wrong with the variety. It met all the requirements, (but) they all agreed the variety should be deregistered. This is unique,” said Grant Watson, head of the agency’s registration program.

Crop Development Centre director Rick Holm said the university will lose the royalty money, but it also spent significant resources and staff time developing Triffid.

“It’s disappointing, but the Crop Development Centre exists to help farmers,” Holm said. “It would have been irresponsible of us to fight to keep it on the market, and face the possibility of our farmers losing an export opportunity.”

Triffid was the first GM crop variety developed by the centre, which registers about a dozen varieties per year. Holm said the centre will not try to develop any more GM varieties because of concerns in Europe and elsewhere.

More than half of all Canadian flax is produced in Saskatchewan, with the remainder grown in Manitoba and Alberta.

—  — – — – – – – – – – – – – – – — – – –  –

http://www.digitaljournal.com/article/280073

Canada’s GM contaminated flax has now been found in 28 countries

By Stephanie Dearing.

Oct 5, 2009 by ■ Stephanie Dearing

After some Canadian flax was found to be contaminated with GM flax in September, it has now been determined that the contamination has affected flax shipped to 28 countries. The contamination means the flax cannot be used as human food.

The finding of GM flax in the Canadian crop in September meant the flax market was not offering good prices, after what was poised to be a very good year for flax farmers. Canadian flax was not being accepted by Europe after the finding of GM flax. The September contamination was found in a German food processing plant. How the GM flax ever contaminated any Canadian crops is a mystery, as the flax has been banned in Canada since 2001. After the finding of CDC Triffid flax, also known as FP697, the European Union issued an alert warning of the GM contamination. GM flax is not legal for sale or consumption in the European Union. Europe normally purchases most of Canada’s flax. At the end of September, the Canadian Flax Council issued a notice that said “The GMO flax issue is a serious problem that is causing significant financial hardship to both Canadian producers and industry and European industry and consumers. The European Union must create a technical solution as an initial step to resolve its zero threshold issue. Canadian flax remains safe for food, feed and processing. This is a regulatory issue, not a safety issue.”

In a press release issued today by the Canadian Biotechnology Action Network (CBAN), the group says 28 countries have now received Canadian flax contaminated with the Triffid strain.

Canadian farmers say that the situation highlights the need for stricter regulations of GM food products in Canada. Organic farmers are concerned that GM crops will affect sales of organic food products because of the risks of cross-contamination.

There is a test available to detect CDC Triffid, and it was approved by the European Union. However, the Canadian Flax Council is waiting for a Canadian university to develop a Canadian test for the GM strain. There is no word as to what, if anything, Food and Agriculture Canada is doing to deal with the issue. However, the agency considers the modified flax as safe for consumption.

In September a commodity trader had categorized the contamination as “blip,” an issue that was blown out of proportion. Larry Weber, owner of Saskatchewan-based Weber Commodities Ltd. told the Star Phoenix that the finding of GM flax in September would not impact Canada’s flax producers beyond a very short time.

The head of the Canadian Flax Council, Barry Hall cautioned the public that the National Research Council’s Saskatoon laboratory is still working to determine the source of the contamination, but speculated that the flax might have been contaminated with GM canola.

Europe had temporarily halted receipt of Canadian flax after finding the contentious GE contamination. There are now fears that Europe might impose a total ban. The Canadian harvest is still underway.

– – – – – —– — – – – – –

http://www.cbc.ca/canada/manitoba/story/2010/01/20/mb-flax-triffid-manitoba.html

“Federal officials are in talks with the EU in hopes of raising its tolerance for genetically modified organisms …”

Read more: http://www.cbc.ca/canada/manitoba/story/2010/01/20/mb-flax-triffid-manitoba.html#ixzz0eKY7gzMe

Triffid seed threatens flax industry

Sep 082009
 

Wikipedia does a good job of drawing the strings together.  The text is below;  please click on the link to see the original, with active links and footnotes:

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

The Bush Six is a term which refers to six former
officials of the United States government under the presidency of George W.
Bush (2001–09), following the filing of criminal charges against them in
Spain.[1][2][3][4][5][6][7][8][9] In March 2009 Baltasar Garzón was asked to
consider whether Spain should allow charges to be filed against:

Alberto Gonzales,
former United States Attorney General and White House Counsel;

John Yoo, of the
Office of Legal Counsel;

Douglas Feith,
former undersecretary of defense for policy;

William Haynes II,
former general counsel for the Department of Defense (chief counsel for Donald
Rumsfeld);

Jay Bybee, also at
the Justice Department’s Office of Legal Counsel; and

David Addington,
former Chief of Staff to the Vice President of the United States (under Dick
Cheney).[10]

Jane Mayer, writing in The New Yorker, reported that
Phillipe Sands had predicted that charges would be laid against the six men
back in his 2008 book Torture Team.[4] Mayer reported that after hearing news
of the Spanish charges, Sands told her, “This is the end of these people’s
professional reputations! This is no joke. We’re talking about the serious
potential deprivation of liberty.”

Scott Horton, writing in The Daily Beast, reported on
April 13, 2009, that his sources said formal charges would be filed on April
14, 2009.[5][11][12] Horton reported that Garzón had been urged to allow
another judge, Ismail Moreno, to conduct the case, because he was still
involved in the possible prosecution of Spanish former Guantanamo captives.
Paul Havens, reporting for the Associated Press reported that an unnamed source
within the Spanish prosecutors office had told him that the charges would be
filed during the week of April 14, 2009.[13] CNN, also quoting an unnamed
source within the Spanish prosecutor’s office, reported that charges were not
expected for several days.[14]

On April 16, 2009, the Spanish Attorney General stated he
thought the Spanish investigative magistrate should drop the consideration of
charges against the six men.[15]

Under the Spanish justice system, investigating
magistrates like Garzón are not under the authority of the Attorney General,
and he can continue to consider laying charges even though the Attorney General
has advised against it.[15]

On April 23, 2009, Eloy Velasco took over responsibility
for determining whether or not the six former Bush officials should face
Spanish charges.[16]

The Guardian reported on April 29, 2009, that Garzón
initiated a formal investigation into whether confessions from four former
Guantanamo captives was the result of the use of abusive interrogation
techniques.[17][18][19] The four men: Hamed Abderrahman Ahmed, Lahcen
Ikassrien, Jamiel Abdul Latif al Banna and Omar Deghayes, had previously faced
charges in Spanish courts, based on confessions they made while in US custody.
Their charges had been dropped based on their claims that their confessions
were false and were the result of abusive interrogation techniques.

On May 5, 2009, Investigating Magistrate Eloy Velasco
formally requested the USA to indicate whether they were going to conduct a
domestic inquiry into the six men’s conduct.[20] Spain’s principle of universal
justice allows third party states to charge non-citizens, and request their
extradition, only when their country of citizenship has not conducted its own
investigation.[20]

On May 20, 2009, the New York Times reported that some
Spanish legislators were proposing a law to strip investigating magistrates of
the authority to pursue international human rights cases.[21] This law,
however, would not retroactively put an end to the progress of current cases.
It would merely have stopped the initiation of similar cases.

According to historian Andy Worthington, writing in the
Huffington Post, Spanish newspaper Público had reported that Garzón was
proceeding to the next phase of his investigation.[22] In February 2011,
Spain’s High Court led by Judge Ruz rejected a Spanish prosecutor’s effort to
stop the investigation. [23]

[edit] U.S. Embassy Cables

Numerous embassy cables leaked by the whistle-blowing
website Wikileaks centered on the progression of the case.[24][25][26] On April
1, 2009 a summary of the case was sent to the U.S. State Department by the
Madrid Embassy. The cable suggests that the U.S. had intended to convince
Spanish Officials to interfere with the National Court’s judicial independence:

we do not know if the government would be willing to take
the risky step of trying behind the scenes to influence the prosecutor’s
recommendation on this case or what their reaction to such a request would
be.[27]

The cable reveals that Chief Prosecutor Javier Zaragoza
intended to steer the case away from its assignment to Judge Baltasar Garzón
who is well known for investigating a universal jurisdiction case targeting
Chilean dictator Augusto Pinochet and has been an outspoken critic of the
Guantanamo Bay detention facility and has publicly stated that former President
George W. Bush should be tried for war crimes.[28] Garzón was “forced to
give up” the case against the Bush Six to another judge who declined to
pursue the investigation.[16][29] Garzón, however, continued an investigation
in to torture at Guantanamo Bay and U.S. Officials indicated in a cable they
feared he may, “attempt to wring all the publicity he can from the case
unless and until he is forced to give it up.” [17]

U.S. Senators, Mel Martinez and Judd Gregg lobbied on behalf
of the U.S. government position as summarized in an embassy cable sent on April
17, 2009. Senator Martinez warned that, “the prosecutions would neither be
understood nor accepted in the U.S. and would have an enormous impact on the
bilateral relationship.” Spanish Foreign Minister Angel Lossada was quoted
as saying, “the National Court had broad jurisdiction for universal
justice and that there was no political influence on the judicial
process.”[30]

Sep 082009
 
  • http://www.andyworthington.co.uk/2009/09/08/spanish-judge-resumes-torture-case-against-six-senior-bush-lawyers/
  • The Spanish newspaper Público reported exclusively on
    Saturday that Judge Baltasar Garzón is pressing ahead with a case against six
    senior Bush administration lawyers for implementing torture at Guantánamo.

    Back in March, Judge Garzón announced that he was
    planning to investigate the six prime architects of the Bush administration’s
    torture policies — former Attorney General Alberto Gonzales; John Yoo, a former
    lawyer in the Justice Department’s Office of Legal Counsel, who played a major
    role in the preparation of the OLC’s notorious “torture memos”; Douglas Feith,
    the former undersecretary of defense for policy; William J. Haynes II, the
    Defense Department’s former general counsel; Jay S. Bybee, Yoo’s superior in
    the OLC, who signed off on the August 2002 “torture memos”; and David
    Addington, former Vice President Dick Cheney‘s Chief of Staff.

    In April, on the advice of the Spanish Attorney General
    Cándido Conde-Pumpido, who believes that an American tribunal should judge the
    case (or dismiss it) before a Spanish court even thinks about becoming
    involved, prosecutors recommended that Judge Garzón should drop his
    investigation. As CNN reported, Mr. Conde-Pumpido told reporters that Judge
    Garzón’s plans threatened to turn the court “into a toy in the hands of people
    who are trying to do a political action.”

    On Saturday, however, Público reported that Judge Garzón
    had accepted a lawsuit presented by a number of Spanish organizations — the
    Asociación Pro Dignidad de los Presos y Presas de España (Organization for the
    Dignity of Spanish Prisoners), Asociación Libre de Abogados (Free Lawyers
    Association), the Asociación Pro Derechos Humanos de España (Association for
    Human Rights in Spain) and Izquierda Unida (a left-wing political party) — and
    three former Guantánamo prisoners (the British residents Jamil El-Banna and
    Omar Deghayes, and Sami El-Laithi, an Egyptian freed in 2005, who was paralyzed
    during an incident involving guards at Guantánamo).

    The newspaper reported that all these groups and
    individuals would take part in any trial, which is somewhat ironic, as,
    although Judge Garzón has been involved in high-profile cases that have
    delighted human rights advocates — his pursuit of General Pinochet, for example
    — he has been severely criticized for his heavy-handed approach to
    terrorism-related cases in Spain (as in the cases of Mohammed Farsi and Farid
    Hilali, amongst others), and, in fact, aggressively pursued an extradition
    request for both Jamil El-Banna and Omar Deghayes on their return from
    Guantánamo to the UK in December 2007, in connection with spurious and
    long-refuted claims about activities related to terrorism, which he was only
    persuaded to drop in March 2008.

    It is, at present, uncertain whether another attempt to
    stifle Judge Garzón will derail him from his pursuit of the Bush
    administration’s lawyers, as he is not known for letting adversaries stand in
    his way. At the end of June, the Spanish Parliament pointedly passed
    legislation aimed at “ending the practice of letting its magistrates seek
    war-crime indictments against officials from any foreign country, including the
    United States,” on the basis that no Spanish Court should be able to judge
    officials of foreign countries except when the victims are Spanish or the
    crimes were committed in Spain.

    However, on Sunday, when Público spoke to Philippe Sands,
    the British lawyer, and author of Torture Team, which provided much of the first-hand
    evidence for Garzón’s case, Sands explicitly stated that there was “no legal
    barrier” to prevent Judge Garzón’s prosecution from proceeding. He explained
    that he believed the recent decision by US Attorney General Eric Holder to
    appoint a special investigator to investigate cases of torture by the CIA is
    related to the Spanish lawsuit and the importance it has acquired because of
    its instigation by Judge Garzón. Sands told Público, “The recent decision by
    Eric Holder emphasizes how appropriate the Spanish investigation is. Many
    commentators believe that this decision has had a significant and direct impact
    in the United States, reminding people that there is an obligation to
    investigate torture.”

    He added, “Judge Garzón’s actions have acted like a catalyst,
    and are supported by many people in the United States, including some members
    of Congress. He has reminded everybody that a blind eye cannot be turned to
    these actions and that there are people who are not going to let that happen.”
    He also explained that Eric Holder’s gesture is only a first step, “limited to
    cases in which interrogators may have exceeded the limits formally approved by
    lawyers in the Justice Department’s Office of Legal Counsel,” that the
    architects of the “legal decisions that purported to justify the use of torture
    are not in immediate danger in the United States,” and that there is,
    therefore, “no legal barrier to the continuation of the Spanish investigation.”

    He concluded by stating that it was “important” that
    Judge Garzón proceeds with the case in Spain, because, although Eric Holder
    “has confirmed the importance of the Convention Against Torture, he has taken
    only a first step that “does not really address the actions of those who were
    truly responsible for its violation.”

    Note: I wish to extend my thanks to Carlos Sardiña
    Galache for alerting me to the latest developments in this important story,
    which was not mentioned in the English-speaking press, and for translating
    crucial passages.

    Aug 122009
     

    We have the power:

    – we are connected

    – we arm each other with knowledge. 

    We can be defeated only if we are kept ignorant, and disconnected from each other. 

    So far, we have been able to thwart Bruce Power from getting its hands on land to build reactors on. 

    SO  Dig in again!  Metis and First Nations people are part of our network. Many of us know someone who knows someone  . . this information will get to the right people if you just send it on – then rack your brain  – – WHO would likely know key people? Maybe you even make a few phone calls. This is urgent. 

    The magic is that we will never know what happened to stop this, the beauty is that all it takes is getting information into people’s hands. 

    The Metis Nation of Saskatchewan is recruiting for a Nuclear Waste Engagement Coordinator.   PLEASE get the word through to people in the Metis Nation.  They should be aware of what their leaders are doing. The only way we have democratic government is if people assume responsibility.  Citizens are responsible for the decisions of their leaders.  Not the other way round.  You can’t whine and cry at bad decisions.  The power is ours.

    http://www.mn-s.ca/  From the website I see that Metis Youth and Metis Women have their own groups within the Metis Nation. They, too, have a responsibility to see that right decisions are made.  

    The experience of the First Nations people at Yucca Mountain should make it clear what’s going on here. 

    The American First Nations used the court system in the U.S. to stop Yucca Mountain (their lands) from becoming the radioactive waste depository for all the radioactive waste in the U.S. 

    President Obama then stepped in and confirmed that Yucca Mountain would be shut down (before it even got going – but AFTER more than $10 billion dollars had been spent on making Yucca Mountain the repository for the waste). 

    The First Nations message was, “You’ve poisoned our water and us through the uranium mines on our lands; you caused disease and death when you exploded test nuclear bombs on our lands.  You are not now going to poison us further by dumping your radioactive waste on our lands.” 

    The Americans are in a bit of a pickle now – no one wants their radioactive waste.  

    Canadians have the same problem, except that we don’t have nearly as much radioactive waste as do the Americans.  

    The pressure is on the Governments to come up with a solution.  Their solution: “We aren’t responsible”.  They created an entity, the NWMO, and said it was their responsibility.   Well – it just so happens that the Governments ARE responsible for seeing that water sources and air aren’t poisoned.  

    Canada set up the “Nuclear Waste Management Organization” – industry people.  The industry uses propaganda and money to buy its way. 

    SO, what do we get?  The Government of Brad Wall sets up the Uranium Development Partnership (UDP) to report.  NO surprise, the industry-stacked Panel recommends radioactive waste disposal in Saskatchewan.  (UPDATE:  the “Dan Perrins” Report on the public consultations on the UDP Report held in summer 2009 showed that the people of Saskatchewan do not want high-level radioactive waste brought here for disposal.)

    The NWMO is meeting in Saskatoon on Sept 16 – 17.  They need a location to dump the radioactive waste from the whole continent – Saskatchewan is the targeted site.

    Experimentation with drilling test burial holes into the Canadian Shield in Manitoba showed that the idea didn’t work. Manitoba therefore passed a law making it illegal to bring radioactive waste from other jurisdictions to Manitoba (legislation, 1987).  Quebec has now passed similar legislation.  

    Back to the Metis Nation:  Besides the Youth and Women’s groups, there’s also a Veterans Group and a Senate as well as the Provincial Council. 

    INFORMATION will win the day.  We all have a responsibility to be well informed and to share the information. We all have a responsibility to see that underground water supplies are not contaminated.  We all have a responsibility not to be naïve, and to speak up. Stop it before it happens.  

    METIS NATION OF SASKATCHEWAN, EXECUTIVE 

    President: Robert G. Doucette

    Vice President:  Allan Morin

    Treasurer: Gabe Lafond

    Secretary: Max Morin 

    The contact info for each is the same:   reception AT  mnsask.ca ; Ph: 306.343.8285

    Please help:  get this information to as many people as possible.  Many thanks!  

    ========================= 

    THE JOB POSTING

    (SaskJobs.ca – Detail for Job Order #5052933.htm) 

    The Metis Nation – Saskatchewan is seeking applications from interested, qualified individuals, particularly those of Metis ancestry, for the position of Waste Engagement Coordinator. 

    The Nuclear Waste Engagement Coordinator (NWEC) will be responsible for coordinating and implementing the Metis Nation-Saskatchewan’s (MN-S) engagement strategy with the Nuclear Waste Management Organization (NWMO).  The NWEC will be in charge of coordinating these engagements in various Metis communities across Saskatchewan, ensuring the budge is adhered too, and fulfilling various reporting requirements throughout the project. 

    If you have a Bachelor Degree with a major or minor in science and have 3 – 5 years working in a science related field, then we invite you to apply for this position. 

    The skills necessary for this position are:

    -Must be capable of working independently

    -Must be proficient in report writing, including technical report writing

    -Must be familiar with the structure of the Metis Nation – Saskatchewan

    -Must have effective communication skills

    -Should have effective problem-solving skills

    -Must have the ability to work within a team environment

    -Must be well organized

    -Must have experience working with budgets

    -Must have knowledge of the nuclear industry 

    The Metis Nation – Saskatchewan thanks all applicants, but only those selected for interviews will be contacted.  The Metis Nation – Saskatchewan reserves the right to hire under an exemption from the Human Rights Commission.   Application Information  Employer Name:

    Metis Nation – Saskatchewan Secretariat Inc.  (contact info)

    Posted Date: 08/05/2009;    Location: SASKATOON;  # of Positions: 1

    Employment Terms: Full Time;  Length of Employment: Contract;  Education: University Bachelor’s Degree

    Experience: 3-5 Years;   Apply By: 08/15/2009

    How to Apply?: Please submit your resume along with a minimum of three references no later than 5:00 p.m. on August 15, 2009

    Aug 012009
     

    There is excellent information about dental amalgams (mercury poisoing) on the International Academy of Oral Medicine and Toxicology’s website.

    From their video library (with thanks to Grant):

    Multiple Sclerosis from Mercury (Silver) Fillings. Linda Brocato testifies before the FDA joint Medical/Dental panel

    http://www.youtube.com/watch?v=9-qhxa-3Wbw

    A google on “Brocato FDA”  brings up numerous reports on the lawsuits against the FDA over its continued stance that amalgams are safe.   There is all the usual corruption of the Government agency by the parties who are on the hook for the liability issues arising out of the poisoning.

    Jul 272009
     

    CONTENTS

    (1)  COMMENTARY

    (2)  VACCINATIONS, DEADLY IMMUNITY BY ROBERT F KENNEDY JR (AUTISM)

    (3)  VIDEO: MAKING A KILLING, THE UNTOLD STORY OF PSYCHOTROPIC DRUGS

    (4)  QUICK, QUIET GENETIC CORN APPROVAL BY THE CFIA

    (5)  MICHAEL MOORE’S SICK-O

    (6)  A MOTHER’S JOURNEY IN HEALING AUTISM BY JENNY MCCARTHY

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

    (1)  COMMENTARY

    Officials from Health Canada, “Healthy Environments and Consumer Safety Programs” met with persons from the environmental network last week. They want to form relationships.

    One of the motivations is to let us know about their “Chemicals Management Plan” so we can support it: (link no longer valid  http://www.chemicalsubstanceschimiques.gc.ca/surveil/index_e.html).  I suppose they recognize that we have healthy communication networks.

    It is encouraging that the Department of Health sees a connection between health and what we are doing in the environment.

    I told them about the multi-disciplinary approach we (our network) took in 2003 when Tony Clement became the Minister of Health:  Health Canada will not reverse the relentlessly upward trend-lines in cancer, developmental problems in children, asthma, and other diseases (which should be the yardstick by which their performance is measured) until they start working with the Departments of Agriculture, Fisheries and Oceans, and Environment.

    I told them it is wonderful that they and all of the environmentalists are working to make things better.

    But I came on strong: nothing will be accomplished until we get the pharmaceutical/chemical/biotech industry out of Government.  Nothing will be accomplished until the Government starts doing its job which is to regulate industry, in the public interest.

    I’ve sent this email to those Health Canada officials, in case they doubt my word.  It is well-documented evidence of what these corporate interests are doing.

    The first article is by Robert F Kennedy Jr., nephew of the slain president of the U.S., son of Robert Kennedy,  who was set to become president but also slain.  People who have been in our network for a few years are familiar with the excellent work of Robert F Kennedy Jr.  He is an environmental lawyer by training, known for setting up the RiverKeepers which became the WaterKeepers.  He has been in Canada on numerous occasions.

    I had the opportunity to hear him speak in Saskatoon at an FSIN Conference.  He is very good at attacking underlying causes of problems.  At that time he was addressing the “externalization of costs”.  Industry is allowed to pass the buck on the environmental and health costs it creates, to the public purse to pay.  Until they are held responsible for these costs, the environmental poisoning will continue.

    Kennedy is a courageous man.  He tackles the issues head-on. He has been working on the pharmaceutical industry and the thimerasol-autism connection for some time. The story of what the pharmaceutical industry has done and continues to do, working with government collaborators, is truly heart-breaking. This is in item #2.

    Item 6 is from the Oprah Winfrey website – mothers of autistic children banding together.  ” Previously, 1 in 500 children was diagnosed with this neurological disorder. Today, Holly says 1 in every 94 boys is affected. For unknown reasons, autism disproportionately affects boys.”

    The evidence pulled together by Robert Kennedy, through access to information, etc. makes it clear that the pharmaceutical industry and American government officials worked together to try and keep the link between autism and thimerasol (ethylmercury) vaccinations under wraps.  They continue to deny and to send the vaccinations to other countries even though they have been stopped here.

    I told the Health Canada officials that my experience over the years with Health Canada, in particular with the Pest Management Regulatory Agency (PMRA), causes me to believe what is documented in the book published earlier this year, “Corrupt to the Core, Memoirs of a Health Canada Scientist” (by Shiv Chopra).  Anybody who has worked to get a municipal pesticide bylaw in place (there are large numbers of such people across Canada) knows just how corrupted Health Canada is.

    I related the story about the full-time government scientist from the PMRA here in Saskatoon who simultaneously is (was?) being paid up to $10,000.00 per contract under hire to CropLife Canada, the lobby-machine for the chemical/biotech/pharmaceutical transnational corporations, the very companies he is supposed to be regulating.

    At the time the situation was brought to light, the relationship between the “doctor” and CropLife had been on-going for 8 years.  When I objected to the conflict-of-interest, I got a letter from a lawyer threatening to sue me for defamation.  I never heard another word from the lawyer after I replied that the mafia uses the threat of broken bones; the chem/biotech corporations are well-known for using the court system to silence people (GMO crops and bovine growth hormone are prime examples).

    I went to Ottawa to meet with the head of the PMRA, Karen Dodds.  She said everything was fine, no problem with the conflict-of-interest because the PMRA has a signed memorandum-of-understanding with Dr. Wolf.

    See item 4.  Monsanto is now partnered with Dow Chemical.  Last week word came out that the CFIA (Canadian Food Inspection Agency – part of Agriculture Canada) and simultaneously the FDA in the U.S. have licensed SmartStax corn. I used this example to (yet again) tell the Government that when the food supply for our society is developed by the criterion that it can be sprayed with chemicals and survive, instead of the criterion of its contribution to our nutritional and health needs, it is pretty obvious that in Government the corporate interest trumps the public interest.  We have “a new genetically-engineered corn with EIGHT different insect- and weed-fighting traits”.

    Health Canada should be in there front and centre, defending our food supply.  Nothing – it is not doing its job. In order to do its job, it has to stand firm against Agriculture Canada. But the “clients” of the PMRA (Health Canada) are the same corporations as are the “clients” of the CFIA (Ag Canada).  The only challenges to defend our food supply have to come from us.  We have a very large, impotent bureaucracy.  And well-placed collaborators with industry.  Read “Corrupt to the Core”.

    Just prior to the announcement of the licensing of SmartStax corn simultaneously by the FDA (U.S.) and the CFIA (Canada), I phoned the new head of the FDA (it was surprisingly easy to reach her office) to register outrage. A lawyer who has worked back and forth between Monsanto and the FDA has been hired by the FDA. The lawyer worked on bovine growth hormone which got registered in the U.S.. In Canada there were whistle-blowers on Monsanto’s attempted bribery of Health Canada officials, one of whom was Shiv Chopra.

    Ad nauseum for old-timers in our network I make the connection:  the pharmaceutical companies own the chemical companies and together they are the biotech corporations. The efforts to “harmonize” the regulations in Canada and the U.S. suggest they also own the governments. Items 2 and 3, following are:

    2.  Robert F Kennedy on the American government working with the pharmaceutical industry, attempted cover-up of the link between thimerasol and autism.  (Thimerasol is used as a preservative in vaccines. It contains ethylmercury. The American government/pharmaceutical corporations continue to supply vaccine containing thimerasol to poorer countries.)  Thanks to Roger for sending in this article.

    3.  Documentary “Making a Killing, the Untold Story of Psychotropic Drugs”. Many thanks to Jackie from Ohio for sending it in.

    I have a special interest in “Making a Killing” because of my experience at Royal University Hospital.  To make a long story shorter, I went to a walk-in clinic after 3 days of stab-like pains in my side.  An x-ray showed a large amount of fluid on my lung.  The doctor didn’t know what to do, and recommended that I come back when doctor so-and-so was on duty, which we jointly determined would be in two days’ time.

    I was very sick but I had a full day to obtain information.  That was a mistake! As a consequence I asked too many questions of the “experts”, the doctors.  Following a Friday afternoon procession of doctors and tests and no answers, I signed a form to get me out of the hospital and went home to do more research.  In the end, when I went back to the hospital, a psychiatrist (maybe she’s a psychologist – I don’t know which) got hold of me.  She determined that I thought I knew more than she did and was hence a danger to myself.  Unbeknownst to me, she diagnosed me as manic, I was forcibly injected with anti-psychotic drugs which caused permanent amnesia of a period of time and I was forced to take more anti-psychotic drugs in pill form, over the next days while I was forcibly confined in the Psychiatric Ward.

    Eventually, a year later, I laid a complaint with the College of Physicians and Surgeons:  my human rights had been seriously infringed upon.  Through the complaint process the doctor-in-question disclosed the name and dosage of the drugs she injected (as part of her defense).

    ~ The internet is wonderful. ~  Using it I was able to show that she not only seriously over-dosed me, but that she did not even know the side effects of the drugs she administered: the one drug almost  always causes loss-of-memory.  She claimed I laid down faulty memory because I was in trauma, nothing to do with the anti-psychotic drug that they held me down to inject.  It was all a very bizarre experience.

    The doctor (Donna Malcolm) stopped the immediate appeal route that is available to people who get locked up in a psychiatric ward by claiming that I had progressed so well under her care that I no longer needed to be locked up, I was being released.  And so she cancelled my appeal hearing. A doctor was coming to testify and had prepared documentation on my behalf, to show that there was nothing wrong with my mind.  I was released to internal medicine after a week of lock-up in the Psych Ward.  I was eventually diagnosed with tuberculosis, fortunately caught in the early stages before it became contagious.

    The College of Physicians and Surgeons later stood by the doctor, in spite of all the evidence. They don’t let you speak and testify to them in person.  . . .  Add it to the list of cases that says self-regulation serves only the industry interest.

    Anyhow – you will understand that I have a special interest in psychotropic drugs.  Actually it pre-dates my direct experience with them.  At the time of the Romanow Commission on Medicare, part of the information I submitted to Romanow was a summary of the work of Dr. Tana Dineen, author of “Manufacturing Victims, What the Psychology Industry Is Doing to People”.   She was a doctor at the University of Saskatchewan.

    Dr Tana Dineen experienced what most people experience when they take on “the system”.  I contacted Tana Dineen a number of years after she wrote her book which takes on the issue of  industrialized mediocare.   At another time I contacted Michael Keating, author of  “To the Last Drop” (1986)  which  contains important documentation of the efforts around making Canadian water into a commodity like oil and gas, the rights to which can be owned by corporations and sold for profit to the U.S.A., the NAFTA story.   Authors who have come under venomous attack because of their books sometimes move onto other work and are happy to leave that chapter of their life in the past.  But back to the issue:

    You can watch “Making a Killing, the Untold Story of Psychotropic Drugs” by going to the video link in item 3.  It tells exactly the same story as Tana Dineen documents in her book, in shorter form, in visual and auditory messaging.

    And by the way, I beat tuberculosis by addressing the question of my immune system- not by using drugs.  Quite a number of you are walking around with the tuberculosis organism.  You’ll never know it because your immune system keeps it in check.

    My reason for combating the organism without drugs is that the drug approach does not make sense.  We know absolutely that resistant tuberculosis has developed and is a deadly problem in Africa and parts of eastern Europe.  The drug companies are trying to find the “next cure”;  but more virulent organisms require more toxic and expensive drugs.  Our bodies can’t handle the increased toxicity, if they find the drugs, AND worse, people in poor countries can’t afford expensive new drugs.  It is such a patently stupid approach – all driven by the drug companies.  The book by John le Carré and film of the same name, “The Constant Gardener” is a chilling story on the same theme, based on true life information.   The book (not the movie) takes the reader to the University of Saskatchewan, as the protagonist tries to track down the people who murdered his wife because of what she learning about the corrupt practices of the pharmaceutical corporations,  in this example in their drive to develop and own the next “cure” for tuberculosis.   Le Carre’s footnotes say that his fictional account is like a pretty Christmas post card in comparison to the real-life corruption of the pharmaceutical corporations.   But back to the main discussion!

    Poverty and other environmental factors compromise immune systems.  If we don’t look after other people, we will be the victims of our own self-centredness.  We create the conditions for diseases to proliferate.

    Item 5. –  Michael Moore’s very funny “Sick-o” is yet another condemnation of the pharmaceutical industry and the myths we are fed.

    – – please circulate widely. The facts in item 2 alone (below), make the heart sick.  I am sending this compendium to one Dean of a Medical School and to the head of one Health District.  I encourage you to send this to every single person you know in the “health” field.

    Passing the email along will help heal your heart.

    /Sandra

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

    (2)  VACCINATIONS, DEADLY IMMUNITY BY ROBERT F KENNEDY JR (AUTISM)(ROLE OF BIG PHARMA)

    Click on  2009-07-25 

    ===========

    (3)  VIDEO: MAKING A KILLING, THE UNTOLD STORY OF PSYCHOTROPIC DRUGS

    Thanks to Jackie from Ohio who writes:

    This is a video worth spending the time watching. There needs to be of an awareness and spreading the word about these things…

    <http://it.truveo.com/Making-A-Killing-The-Untold-Story-Of-Psychotropic/id/817313309>

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

    (4)  QUICK, QUIET GENETIC CORN APPROVAL BY THE CFIA

    2009-07-25  Quick & Quiet, Canadian Food Inspection Agency (CFIA)  approved a new genetically engineered corn with eight different insect- and weed-fighting traits (“Smartstax”), Montreal Gazette

     

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

    (5)  MICHAEL MOORE’S SICK-O

    A number of excerpts from his documentary can be seen on YouTube.  Here’s a couple.  I have to rent the complete video!

    a.

    http://www.youtube.com/watch?v=xlDAUKSh9CQ&eurl=http%3A%2F%2Fvideo%2Egoogle%2Eca%2Fvideosearch%3Fhl%3Den%26q%3Dmichael%2Bmoore%2Bsick%2Do%26um%3D1%26ie%3DUTF%2D8%26ei%3DLTFuSoOAHMGFtge9kPmIDA%26sa%3DX%26oi%3Dvideo%5Fresult%5Fgro&feature=player_embedded

    b.  http://video.google.ca/videosearch?hl=en&q=michael+moore+sick-o&um=1&ie=UTF-8&ei=LTFuSoOAHMGFtge9kPmIDA&sa=X&oi=video_result_group&ct=title&resnum=4#

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

    (6)  A MOTHER’S JOURNEY IN HEALING AUTISM BY JENNY MCCARTHY

    (UPDATE:   two youtubes featuring Jenny McCarthy, one on Larry King Live.  I suspect that Big Pharma is doing as much as it can to put Mc Carthy in a bad light because she is convincing.   http://www.youtube.com/watch?v=qGW4a96GqGc&feature=related   and   http://www.youtube.com/watch?v=HX-SCdjDOrA.   Consider what she has to say, in light of all the other evidence to back her up.  Many doctors, for example those who deny all the evidence,  have lost credibility.)

    In her new book, Louder Than Words: A Mother’s Journey in Healing Autism, actress Jenny McCarthy shares her emotional story of diagnosis, hope, …

    Excerpt from  http://www.oprah.com/slideshow/oprahshow/oprahshow1_ss_20070918/5

    . ….  In recent years, the number of children diagnosed with autism has risen from 1 in every 500 children to 1 in 150 — and science has not discovered a reason why. Jenny says she believes that childhood vaccinations may play a part. “What number will it take for people just to start listening to what the mothers of children who have seen autism have been saying for years, which is, ‘We vaccinated our baby and something happened.”

    Jenny says even before Evan received his vaccines, she tried to talk to her pediatrician about it. “Right before his MMR shot, I said to the doctor, ‘I have a very bad feeling about this shot. This is the autism shot, isn’t it?’ And he said, ‘No, that is ridiculous. It is a mother’s desperate attempt to blame something,’ and he swore at me, and then the nurse gave [Evan] the shot,” she says. “And I remember going, ‘Oh, God, I hope he’s right.’ And soon thereafter—boom—the soul’s gone from his eyes.”

    Despite her belief, Jenny says she is not against vaccines. “I am all for them, but there needs to be a safer vaccine schedule. There needs to be something done. The fact that the [Centers for Disease Control and Prevention] acts as if these vaccines are one size fits all is just crazy to me,” she says. “People need to start listening to what the moms have been saying.”

    We contacted the Centers for Disease Control and Prevention about whether there is a link between autism and vaccines and they gave us the following statement:

    “CDC places a high priority on vaccine safety and the integrity and credibility of its vaccine safety research. This commitment not only stems from our scientific and medical dedication, it is also personal—for most of us who work at CDC are also parents and grandparents. And as such, we too, have high levels of personal interest and concern in the health and safety of children, families and communities. We simply don’t know what causes most cases of autism, but we’re doing everything we can to find out. The vast majority of science to date does not support an association between thimerosal in vaccines and autism. But we are currently conducting additional studies to further determine what role, if any, thimerosal in vaccines may play in the development of autism. It is important to remember, vaccines protect and save lives. Vaccines protect infants, children and adults from the unnecessary harm and premature death caused by vaccine-preventable diseases.”

    …  Previously, 1 in 500 children was diagnosed with this neurological disorder. Today, Holly says 1 in every 94 boys is affected. For unknown reasons, autism disproportionately affects boys.

    Jul 252009
     

    the most genes artificially added to a single plant was three, but Smartstax includes eight

    These are eight poisons built into the genome of the corn.   Genes do not wash off.

     

    QUICK, QUIET GENETIC CORN APPROVAL BY THE CFIA

    To see the CFIA documentation on the approval for Smartstax corn, go to:  2013-05-28  Dismay when people realize connection between GMO corn and tacos, tortillas, corn chips (corn meal).

    Earlier, on corn see:  2004-06-14   Another big hit – $112 million pay out over Contamination of Corn (Aventis StarLink corn)

     

    We’ve done a lot of work on GMO crops, our food supply.

    This recent development made me so mad I phoned Carole Swan, President of the CFIA and gave them a piece of my mind.

    I later talked with Lucy Sharratt who is dedicated to GMO’s at CBAN (Canadian Biotechnology Action Network).  Numbers of other people have phoned Carole Swan.  Lucy’s reading on the situation is that the CFIA is getting nervous.  I am sure that a phone call from you will add to their nervousness:

    Carole Swan

    President of the CFIA

    (613) 773-6000

    swanc@inspection.gc.ca

    (613) 773-5762

    Sherry – Exec Asst

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

    “SMARTSTAX” CORN

    Smartstax corn was approved on the same day in Canada, as in the U.S.   Which is to say that the “harmonization” of regulation that the industry has been working on is now in place.  (Canada established an independent approval process after the IBT Laboratory Scandals in the U.S. in the 1980s.  Monsanto played a role.  By 2009 they have effectively removed the “independent” approval system in Canada.)

    From Wikipedia – info obviously from Monsanto/Dow themselves.:

    SmartStax is a brand of genetically modified seed made through a collaboration between Monsanto Company and Dow.[1] It takes advantage of multiple modes of insect protection and herbicide tolerance. SmartStax takes advantage of Yieldgard VT Triple (Monsanto), Herculex Xtra (Dow), RoundUp Ready 2 (Monsanto), and Liberty Link (Dow). The traits included protect against above-ground insects, Below-Ground insects, and provide broad herbicide tolerance. It is currently available for corn, but cotton, soybean, and specialty crop variations are to be released. Previously, the most genes artificially added to a single plant was three, but Smartstax includes eight. Smartstax also takes advantage of the Acceleron Seed Treatment System which protects against insects at the earliest stages of development. SmartStax is ground-breaking in that it requires only 5% refuge acres as opposed to the 20% required of older technologies. Smartstax builds towards Monsanto’s Promise of doubling yields by 2030 on the same or less land.[2] Smartstax is sold under the Genuity (Monsanto) and Mycogen (Dow) brands.

     

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

    Quick, quiet genetic corn approval questioned

    By Michelle Lalonde

    Montreal Gazette via Canwest News Service

    July 25, 2009

    MONTREAL — The Canadian Food Inspection Agency has quietly approved a new genetically engineered corn with eight different insect- and weed-fighting traits, but farmer and environmental groups in Canada say the approval was rushed and environmental risks ignored.

    Developed through a research agreement between Monsanto and Dow AgroSciences, SmartStax corn is unique in that it “stacks” eight different genetically engineered traits that will allow corn to tolerate certain weed- and insect-killing products made by the two companies.

    Each of the eight traits has been individually approved by the CFIA, but opponents are concerned there might be unintended consequences when the traits are combined.

    “You’d think that a combination of eight GE traits would trigger an environmental assessment, but the CFIA has (provided) no public record of their evaluation,” said Lucy Sharratt, co-ordinator of the Canadian Biotechnology Action Network.

    The CFIA has also conditionally authorized for SmartStax a reduction in the size of the buffer zone, or “refuge,” normally required around genetically engineered corn.

    Farmers who grow insect-resistant corn have to plant regular corn around it in an area equal to 20 per cent of the GE cornfield. This is to delay the evolution of insect resistance to the toxins in the GE corn, which would then necessitate the use of stronger pesticides.

    CFIA officials were not available for comment Friday. A short statement on its website said “the CFIA has evaluated the potential impact on and risk to the environment of using a 5 per cent non-Bt refuge strategy for this product, and has concluded that a conditional authorization until Dec. 31, 2012, of the use of this refuge poses minimal risk to the environment.”

    “Not only did the CFIA neglect to do a risk evaluation for SmartStax corn, but it has also seriously reduced one of the only precautions imposed on farmers,” said Benoit Girouard of Quebec’s Union Paysanne, a farmers’ group.

    Between now and December 2012, the CFIA statement said, Monsanto and Dow are required to evaluate how insects like corn rootworm are adapting to the product.

    “It’s like putting the wolf in charge of the sheep’s welfare,” said Eric Darier, director of Greenpeace Quebec.

    In May, the American Academy of Environmental Medicine called for an immediate moratorium on genetically modified foods, saying they pose a “serious health risk.”

    Jul 252009
     

    Please see  2011-01-28 for a summary of  mercury poisoning from dental amalgams and vaccinations that contain ethyl mercury.

    VACCINATIONS, DEADLY IMMUNITY BY ROBERT F KENNEDY JR (AUTISM) 

    http://www.infowars.com/vaccinations-deadly-immunity/   

    Vaccinations: Deadly Immunity

    Robert F. Kennedy Jr.

    Global Research

    July 25, 2009 

    In June 2000, a group of top government scientists and health officials gathered for a meeting at the isolated Simpsonwood conference center in Norcross, Georgia. Convened by the Centers for Disease Control and Prevention, the meeting was held at this Methodist retreat center, nestled in wooded farmland next to the Chattahoochee River, to ensure complete secrecy. The agency had issued no public announcement of the session — only private invitations to fifty-two attendees. There were high-level officials from the CDC and the Food and Drug Administration, the top vaccine specialist from the World Health Organization in Geneva and representatives of every major vaccine manufacturer, including GlaxoSmithKline, Merck, Wyeth and Aventis Pasteur. All of the scientific data under discussion, CDC officials repeatedly reminded the participants, was strictly “embargoed.” There would be no making photocopies of documents, no taking papers with them when they left.  

    Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans. 

    The federal officials and industry representatives had assembled to discuss a disturbing new study that raised alarming questions about the safety of a host of common childhood vaccines administered to infants and young children. According to a CDC epidemiologist named Tom Verstraeten, who had analyzed the agency’s massive database containing the medical records of 100,000 children, a mercury-based preservative in the vaccines — thimerosal — appeared to be responsible for a dramatic increase in autism and a host of other neurological disorders among children. “I was actually stunned by what I saw,” Verstraeten told those assembled at Simpsonwood, citing the staggering number of earlier studies that indicate a link between thimerosal and speech delays, attention-deficit disorder, hyperactivity and autism. Since 1991, when the CDC and the FDA had recommended that three additional vaccines laced with the preservative be given to extremely young infants — in one case, within hours of birth — the estimated number of cases of autism had increased fifteenfold, from one in every 2,500 children to one in 166 children.

    Even for scientists and doctors accustomed to confronting issues of life and death, the findings were frightening. “You can play with this all you want,” Dr. Bill Weil, a consultant for the American Academy of Pediatrics, told the group. The results “are statistically significant.” Dr. Richard Johnston, an immunologist and pediatrician from the University of Colorado whose grandson had been born early on the morning of the meeting’s first day, was even more alarmed. “My gut feeling?” he said. “Forgive this personal comment — I do not want my grandson to get a thimerosal-containing vaccine until we know better what is going on.” 

    But instead of taking immediate steps to alert the public and rid the vaccine supply of thimerosal, the officials and executives at Simpsonwood spent most of the next two days discussing how to cover up the damaging data. According to transcripts obtained under the Freedom of Information Act, many at the meeting were concerned about how the damaging revelations about thimerosal would affect the vaccine industry’s bottom line. “We are in a bad position from the standpoint of defending any lawsuits,” said Dr. Robert Brent, a pediatrician at the Alfred I. duPont Hospital for Children in Delaware. “This will be a resource to our very busy plaintiff attorneys in this country.” Dr. Bob Chen, head of vaccine safety for the CDC, expressed relief that “given the sensitivity of the information, we have been able to keep it out of the hands of, let’s say, less responsible hands.” Dr. John Clements, vaccines advisor at the World Health Organization, declared that “perhaps this study should not have been done at all.” He added that “the research results have to be handled,” warning that the study “will be taken by others and will be used in other ways beyond the control of this group.” 

    In fact, the government has proved to be far more adept at handling the damage than at protecting children’s health. The CDC paid the Institute of Medicine to conduct a new study to whitewash the risks of thimerosal, ordering researchers to “rule out” the chemical’s link to autism. It withheld Verstraeten’s findings, even though they had been slated for immediate publication, and told other scientists that his original data had been “lost” and could not be replicated. And to thwart the Freedom of Information Act, it handed its giant database of vaccine records over to a private company, declaring it off-limits to researchers. By the time Verstraeten finally published his study in 2003, he had gone to work for GlaxoSmithKline and reworked his data to bury the link between thimerosal and autism. 

    Vaccine manufacturers had already begun to phase thimerosal out of injections given to American infants — but they continued to sell off their mercury-based supplies of vaccines until last year. The CDC and FDA gave them a hand, buying up the tainted vaccines for export to developing countries and allowing drug companies to continue using the preservative in some American vaccines — including several pediatric flu shots as well as tetanus boosters routinely given to eleven-year-olds.

    The drug companies are also getting help from powerful lawmakers in Washington. Senate Majority Leader Bill Frist, who has received $873,000 in contributions from the pharmaceutical industry, has been working to immunize vaccine makers from liability in 4,200 lawsuits that have been filed by the parents of injured children. On five separate occasions, Frist has tried to seal all of the government’s vaccine-related documents — including the Simpsonwood transcripts — and shield Eli Lilly, the developer of thimerosal, from subpoenas. In 2002, the day after Frist quietly slipped a rider known as the “Eli Lilly Protection Act” into a homeland security bill, the company contributed $10,000 to his campaign and bought 5,000 copies of his book on bioterrorism. The measure was repealed by Congress in 2003 — but earlier this year, Frist slipped another provision into an anti-terrorism bill that would deny compensation to children suffering from vaccine-related brain disorders. “The lawsuits are of such magnitude that they could put vaccine producers out of business and limit our capacity to deal with a biological attack by terrorists,” says Dean Rosen, health policy adviser to Frist. 

    Even many conservatives are shocked by the government’s effort to cover up the dangers of thimerosal. Rep. Dan Burton, a Republican from Indiana, oversaw a three-year investigation of thimerosal after his grandson was diagnosed with autism. “Thimerosal used as a preservative in vaccines is directly related to the autism epidemic,” his House Government Reform Committee concluded in its final report. “This epidemic in all probability may have been prevented or curtailed had the FDA not been asleep at the switch regarding a lack of safety data regarding injected thimerosal, a known neurotoxin.” The FDA and other public-health agencies failed to act, the committee added, out of “institutional malfeasance for self protection” and “misplaced protectionism of the pharmaceutical industry.” 

    The story of how government health agencies colluded with Big Pharma to hide the risks of thimerosal from the public is a chilling case study of institutional arrogance, power and greed. I was drawn into the controversy only reluctantly. As an attorney and environmentalist who has spent years working on issues of mercury toxicity, I frequently met mothers of autistic children who were absolutely convinced that their kids had been injured by vaccines. Privately, I was skeptical.

    I doubted that autism could be blamed on a single source, and I certainly understood the government’s need to reassure parents that vaccinations are safe; the eradication of deadly childhood diseases depends on it. I tended to agree with skeptics like Rep. Henry Waxman, a Democrat from California, who criticized his colleagues on the House Government Reform Committee for leaping to conclusions about autism and vaccinations. “Why should we scare people about immunization,” Waxman pointed out at one hearing, “until we know the facts?”

    It was only after reading the Simpsonwood transcripts, studying the leading scientific research and talking with many of the nation’s pre-eminent authorities on mercury that I became convinced that the link between thimerosal and the epidemic of childhood neurological disorders is real. Five of my own children are members of the Thimerosal Generation — those born between 1989 and 2003 — who received heavy doses of mercury from vaccines. “The elementary grades are overwhelmed with children who have symptoms of neurological or immune-system damage,” Patti White, a school nurse, told the House Government Reform Committee in 1999. “Vaccines are supposed to be making us healthier; however, in twenty-five years of nursing I have never seen so many damaged, sick kids. Something very, very wrong is happening to our children.”

    More than 500,000 kids currently suffer from autism, and pediatricians diagnose more than 40,000 new cases every year. The disease was unknown until 1943, when it was identified and diagnosed among eleven children born in the months after thimerosal was first added to baby vaccines in 1931.

    Some skeptics dispute that the rise in autism is caused by thimerosal-tainted vaccinations. They argue that the increase is a result of better diagnosis — a theory that seems questionable at best, given that most of the new cases of autism are clustered within a single generation of children. “If the epidemic is truly an artifact of poor diagnosis,” scoffs Dr. Boyd Haley, one of the world’s authorities on mercury toxicity, “then where are all the twenty-year-old autistics?” Other researchers point out that Americans are exposed to a greater cumulative “load” of mercury than ever before, from contaminated fish to dental fillings, and suggest that thimerosal in vaccines may be only part of a much larger problem. It’s a concern that certainly deserves far more attention than it has received — but it overlooks the fact that the mercury concentrations in vaccines dwarf other sources of exposure to our children.

    What is most striking is the lengths to which many of the leading detectives have gone to ignore — and cover up — the evidence against thimerosal. From the very beginning, the scientific case against the mercury additive has been overwhelming. The preservative, which is used to stem fungi and bacterial growth in vaccines, contains ethylmercury, a potent neurotoxin. Truckloads of studies have shown that mercury tends to accumulate in the brains of primates and other animals after they are injected with vaccines — and that the developing brains of infants are particularly susceptible. In 1977, a Russian study found that adults exposed to much lower concentrations of ethylmercury than those given to American children still suffered brain damage years later. Russia banned thimerosal from children’s vaccines twenty years ago, and Denmark, Austria, Japan, Great Britain and all the Scandinavian countries have since followed suit.

    “You couldn’t even construct a study that shows thimerosal is safe,” says Haley, who heads the chemistry department at the University of Kentucky. “It’s just too darn toxic. If you inject thimerosal into an animal, its brain will sicken. If you apply it to living tissue, the cells die. If you put it in a petri dish, the culture dies. Knowing these things, it would be shocking if one could inject it into an infant without causing damage.”

    Internal documents reveal that Eli Lilly, which first developed thimerosal, knew from the start that its product could cause damage — and even death — in both animals and humans. In 1930, the company tested thimerosal by administering it to twenty-two patients with terminal meningitis, all of whom died within weeks of being injected — a fact Lilly didn’t bother to report in its study declaring thimerosal safe. In 1935, researchers at another vaccine manufacturer, Pittman-Moore, warned Lilly that its claims about thimerosal’s safety “did not check with ours.” Half the dogs Pittman injected with thimerosal-based vaccines became sick, leading researchers there to declare the preservative “unsatisfactory as a serum intended for use on dogs.”

    In the decades that followed, the evidence against thimerosal continued to mount. During the Second World War, when the Department of Defense used the preservative in vaccines on soldiers, it required Lilly to label it “poison.” In 1967, a study in Applied Microbiology found that thimerosal killed mice when added to injected vaccines. Four years later, Lilly’s own studies discerned that thimerosal was “toxic to tissue cells” in concentrations as low as one part per million — 100 times weaker than the concentration in a typical vaccine. Even so, the company continued to promote thimerosal as “nontoxic” and also incorporated it into topical disinfectants. In 1977, ten babies at a Toronto hospital died when an antiseptic preserved with thimerosal was dabbed onto their umbilical cords.

    In 1982, the FDA proposed a ban on over-the-counter products that contained thimerosal, and in 1991 the agency considered banning it from animal vaccines. But tragically, that same year, the CDC recommended that infants be injected with a series of mercury-laced vaccines. Newborns would be vaccinated for hepatitis B within twenty-four hours of birth, and two-month-old infants would be immunized for haemophilus influenzae B and diphtheria-tetanus-pertussis.

    The drug industry knew the additional vaccines posed a danger. The same year that the CDC approved the new vaccines, Dr. Maurice Hilleman, one of the fathers of Merck’s vaccine programs, warned the company that six-month-olds who were administered the shots would suffer dangerous exposure to mercury. He recommended that thimerosal be discontinued, “especially when used on infants and children,” noting that the industry knew of nontoxic alternatives. “The best way to go,” he added, “is to switch to dispensing the actual vaccines without adding preservatives.”

    For Merck and other drug companies, however, the obstacle was money. Thimerosal enables the pharmaceutical industry to package vaccines in vials that contain multiple doses, which require additional protection because they are more easily contaminated by multiple needle entries. The larger vials cost half as much to produce as smaller, single-dose vials, making it cheaper for international agencies to distribute them to impoverished regions at risk of epidemics. Faced with this “cost consideration,” Merck ignored Hilleman’s warnings, and government officials continued to push more and more thimerosal-based vaccines for children. Before 1989, American preschoolers received eleven vaccinations — for polio, diphtheria-tetanus-pertussis and measles-mumps-rubella. A decade later, thanks to federal recommendations, children were receiving a total of twenty-two immunizations by the time they reached first grade. 

    As the number of vaccines increased, the rate of autism among children exploded. During the 1990s, 40 million children were injected with thimerosal-based vaccines, receiving unprecedented levels of mercury during a period critical for brain development. Despite the well-documented dangers of thimerosal, it appears that no one bothered to add up the cumulative dose of mercury that children would receive from the mandated vaccines. “What took the FDA so long to do the calculations?” Peter Patriarca, director of viral products for the agency, asked in an e-mail to the CDC in 1999. “Why didn’t CDC and the advisory bodies do these calculations when they rapidly expanded the childhood immunization schedule?” 

    But by that time, the damage was done. At two months, when the infant brain is still at a critical stage of development, infants routinely received three inoculations that contained a total of 62.5 micrograms of ethylmercury — a level 99 times greater than the EPA’s limit for daily exposure to methylmercury, a related neurotoxin. Although the vaccine industry insists that ethylmercury poses little danger because it breaks down rapidly and is removed by the body, several studies — including one published in April by the National Institutes of Health — suggest that ethylmercury is actually more toxic to developing brains and stays in the brain longer than methylmercury. 

    Officials responsible for childhood immunizations insist that the additional vaccines were necessary to protect infants from disease and that thimerosal is still essential in developing nations, which, they often claim, cannot afford the single-dose vials that don’t require a preservative. Dr. Paul Offit, one of CDC’s top vaccine advisers, told me, “I think if we really have an influenza pandemic — and certainly we will in the next twenty years, because we always do — there’s no way on God’s earth that we immunize 280 million people with single-dose vials. There has to be multidose vials.” 

    But while public-health officials may have been well-intentioned, many of those on the CDC advisory committee who backed the additional vaccines had close ties to the industry. Dr. Sam Katz, the committee’s chair, was a paid consultant for most of the major vaccine makers and was part of a team that developed the measles vaccine and brought it to licensure in 1963. Dr. Neal Halsey, another committee member, worked as a researcher for the vaccine companies and received honoraria from Abbott Labs for his research on the hepatitis B vaccine. 

    Indeed, in the tight circle of scientists who work on vaccines, such conflicts of interest are common. Rep. Burton says that the CDC “routinely allows scientists with blatant conflicts of interest to serve on intellectual advisory committees that make recommendations on new vaccines,” even though they have “interests in the products and companies for which they are supposed to be providing unbiased oversight.” The House Government Reform Committee discovered that four of the eight CDC advisers who approved guidelines for a rotavirus vaccine “had financial ties to the pharmaceutical companies that were developing different versions of the vaccine.” 

    Offit, who shares a patent on one of the vaccines, acknowledged to me that he “would make money” if his vote eventually leads to a marketable product. But he dismissed my suggestion that a scientist’s direct financial stake in CDC approval might bias his judgment. “It provides no conflict for me,” he insists. “I have simply been informed by the process, not corrupted by it. When I sat around that table, my sole intent was trying to make recommendations that best benefited the children in this country. It’s offensive to say that physicians and public-health people are in the pocket of industry and thus are making decisions that they know are unsafe for children. It’s just not the way it works.” 

    Other vaccine scientists and regulators gave me similar assurances. Like Offit, they view themselves as enlightened guardians of children’s health, proud of their “partnerships” with pharmaceutical companies, immune to the seductions of personal profit, besieged by irrational activists whose anti-vaccine campaigns are endangering children’s health. They are often resentful of questioning. “Science,” says Offit, “is best left to scientists.” 

    Still, some government officials were alarmed by the apparent conflicts of interest. In his e-mail to CDC administrators in 1999, Paul Patriarca of the FDA blasted federal regulators for failing to adequately scrutinize the danger posed by the added baby vaccines. “I’m not sure there will be an easy way out of the potential perception that the FDA, CDC and immunization-policy bodies may have been asleep at the switch re: thimerosal until now,” Patriarca wrote. The close ties between regulatory officials and the pharmaceutical industry, he added, “will also raise questions about various advisory bodies regarding aggressive recommendations for use” of thimerosal in child vaccines. 

    If federal regulators and government scientists failed to grasp the potential risks of thimerosal over the years, no one could claim ignorance after the secret meeting at Simpsonwood. But rather than conduct more studies to test the link to autism and other forms of brain damage, the CDC placed politics over science. The agency turned its database on childhood vaccines — which had been developed largely at taxpayer expense — over to a private agency, America’s Health Insurance Plans, ensuring that it could not be used for additional research. It also instructed the Institute of Medicine, an advisory organization that is part of the National Academy of Sciences, to produce a study debunking the link between thimerosal and brain disorders. The CDC “wants us to declare, well, that these things are pretty safe,” Dr. Marie McCormick, who chaired the IOM’s Immunization Safety Review Committee, told her fellow researchers when they first met in January 2001. “We are not ever going to come down that [autism] is a true side effect” of thimerosal exposure. According to transcripts of the meeting, the committee’s chief staffer, Kathleen Stratton, predicted that the IOM would conclude that the evidence was “inadequate to accept or reject a causal relation” between thimerosal and autism. That, she added, was the result “Walt wants” — a reference to Dr. Walter Orenstein, director of the National Immunization Program for the CDC. 

    For those who had devoted their lives to promoting vaccination, the revelations about thimerosal threatened to undermine everything they had worked for. “We’ve got a dragon by the tail here,” said Dr. Michael Kaback, another committee member. “The more negative that [our] presentation is, the less likely people are to use vaccination, immunization — and we know what the results of that will be. We are kind of caught in a trap. How we work our way out of the trap, I think is the charge.” 

    Even in public, federal officials made it clear that their primary goal in studying thimerosal was to dispel doubts about vaccines. “Four current studies are taking place to rule out the proposed link between autism and thimerosal,” Dr. Gordon Douglas, then-director of strategic planning for vaccine research at the National Institutes of Health, assured a Princeton University gathering in May 2001. “In order to undo the harmful effects of research claiming to link the [measles] vaccine to an elevated risk of autism, we need to conduct and publicize additional studies to assure parents of safety.” Douglas formerly served as president of vaccinations for Merck, where he ignored warnings about thimerosal’s risks. 

    In May of last year, the Institute of Medicine issued its final report. Its conclusion: There is no proven link between autism and thimerosal in vaccines. Rather than reviewing the large body of literature describing the toxicity of thimerosal, the report relied on four disastrously flawed epidemiological studies examining European countries, where children received much smaller doses of thimerosal than American kids. It also cited a new version of the Verstraeten study, published in the journal Pediatrics, that had been reworked to reduce the link between thimerosal and autism. The new study included children too young to have been diagnosed with autism and overlooked others who showed signs of the disease. The IOM declared the case closed and — in a startling position for a scientific body — recommended that no further research be conducted. 

    The report may have satisfied the CDC, but it convinced no one. Rep. David Weldon, a Republican physician from Florida who serves on the House Government Reform Committee, attacked the Institute of Medicine, saying it relied on a handful of studies that were “fatally flawed” by “poor design” and failed to represent “all the available scientific and medical research.” CDC officials are not interested in an honest search for the truth, Weldon told me, because “an association between vaccines and autism would force them to admit that their policies irreparably damaged thousands of children. Who would want to make that conclusion about themselves?” 

    Under pressure from Congress and parents, the Institute of Medicine convened another panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program. In February, the new panel, composed of different scientists, criticized the way the VSD had been used in the Verstraeten study, and urged the CDC to make its vaccine database available to the public. 

    So far, though, only two scientists have managed to gain access. Dr. Mark Geier, president of the Genetics Center of America, and his son, David, spent a year battling to obtain the medical records from the CDC. Since August 2002, when members of Congress pressured the agency to turn over the data, the Geiers have completed six studies that demonstrate a powerful correlation between thimerosal and neurological damage in children. One study, which compares the cumulative dose of mercury received by children born between 1981 and 1985 with those born between 1990 and 1996, found a “very significant relationship” between autism and vaccines. Another study of educational performance found that kids who received higher doses of thimerosal in vaccines were nearly three times as likely to be diagnosed with autism and more than three times as likely to suffer from speech disorders and mental retardation. Another soon-to-be published study shows that autism rates are in decline following the recent elimination of thimerosal from most vaccines. 

    As the federal government worked to prevent scientists from studying vaccines, others have stepped in to study the link to autism. In April, reporter Dan Olmsted of UPI undertook one of the more interesting studies himself. Searching for children who had not been exposed to mercury in vaccines — the kind of population that scientists typically use as a “control” in experiments — Olmsted scoured the Amish of Lancaster County, Pennsylvania, who refuse to immunize their infants. Given the national rate of autism, Olmsted calculated that there should be 130 autistics among the Amish. He found only four. One had been exposed to high levels of mercury from a power plant. The other three — including one child adopted from outside the Amish community — had received their vaccines.

    At the state level, many officials have also conducted in-depth reviews of thimerosal. While the Institute of Medicine was busy whitewashing the risks, the Iowa legislature was carefully combing through all of the available scientific and biological data. “After three years of review, I became convinced there was sufficient credible research to show a link between mercury and the increased incidences in autism,” says state Sen. Ken Veenstra, a Republican who oversaw the investigation. “The fact that Iowa’s 700 percent increase in autism began in the 1990s, right after more and more vaccines were added to the children’s vaccine schedules, is solid evidence alone.” Last year, Iowa became the first state to ban mercury in vaccines, followed by California. Similar bans are now under consideration in thirty-two other states.

    But instead of following suit, the FDA continues to allow manufacturers to include thimerosal in scores of over-the-counter medications as well as steroids and injected collagen. Even more alarming, the government continues to ship vaccines preserved with thimerosal to developing countries — some of which are now experiencing a sudden explosion in autism rates. In China, where the disease was virtually unknown prior to the introduction of thimerosal by U.S. drug manufacturers in 1999, news reports indicate that there are now more than 1.8 million autistics. Although reliable numbers are hard to come by, autistic disorders also appear to be soaring in India, Argentina, Nicaragua and other developing countries that are now using thimerosal-laced vaccines. The World Health Organization continues to insist thimerosal is safe, but it promises to keep the possibility that it is linked to neurological disorders “under review.” 

    I devoted time to study this issue because I believe that this is a moral crisis that must be addressed. If, as the evidence suggests, our public-health authorities knowingly allowed the pharmaceutical industry to poison an entire generation of American children, their actions arguably constitute one of the biggest scandals in the annals of American medicine. “The CDC is guilty of incompetence and gross negligence,” says Mark Blaxill, vice president of Safe Minds, a nonprofit organization concerned about the role of mercury in medicines. “The damage caused by vaccine exposure is massive. It’s bigger than asbestos, bigger than tobacco, bigger than anything you’ve ever seen.”

    It’s hard to calculate the damage to our country — and to the international efforts to eradicate epidemic diseases — if Third World nations come to believe that America’s most heralded foreign-aid initiative is poisoning their children. It’s not difficult to predict how this scenario will be interpreted by America’s enemies abroad. The scientists and researchers — many of them sincere, even idealistic — who are participating in efforts to hide the science on thimerosal claim that they are trying to advance the lofty goal of protecting children in developing nations from disease pandemics. They are badly misguided. Their failure to come clean on thimerosal will come back horribly to haunt our country and the world’s poorest populations. 

    Global Research comments: This story has been updated to correct several inaccuracies in the original, published version. As originally reported, American preschoolers received only three vaccinations before 1989, but the article failed to note that they were innoculated a total of eleven times with those vaccines, including boosters. The article also misstated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms – an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury. Finally, because of an editing error, the article misstated the contents of the rotavirus vaccine approved by the CDC. It did not contain thimerosal. Salon and Rolling Stone regret the errors. 

    An earlier version of this story stated that the Institute of Medicine convened a second panel to review the work of the Immunization Safety Review Committee that had found no evidence of a link between thimerosal and autism. In fact, the IOM convened the second panel to address continuing concerns about the Vaccine Safety Datalink Data Sharing program, including those raised by critics of the IOM’s earlier work. But the panel was not charged with reviewing the committee’s findings. The story also inadvertently omitted a word and transposed two sentences in a quote by Dr. John Clements, and incorrectly stated that Dr. Sam Katz held a patent with Merck on the measles vaccine. In fact, Dr. Katz was part of a team that developed the vaccine and brought it to licensure, but he never held the patent. Salon and Rolling Stone regret the errors. 

    CLARIFICATION: After publication of this story, Salon and Rolling Stone corrected an error that misstated the level of ethylmercury received by infants injected with all their shots by the age of six months. It was 187 micrograms ? an amount forty percent, not 187 times, greater than the EPA’s limit for daily exposure to methylmercury. At the time of the correction, we were aware that the comparison itself was flawed, but as journalists we considered it more appropriate to state the correct figure rather than replace it with another number entirely. 

    Since that earlier correction, however, it has become clear from responses to the article that the forty-percent number, while accurate, is misleading. It measures the total mercury load an infant received from vaccines during the first six months, calculates the daily average received based on average body weight, and then compares that number to the EPA daily limit. But infants did not receive the vaccines as a ?daily average? ? they received massive doses on a single day, through multiple shots. As the story states, these single-day doses exceeded the EPA limit by as much as 99 times. Based on the misunderstanding, and to avoid further confusion, we have amended the story to eliminate the forty-percent figure. 

    Correction: The story misattributed a quote to Andy Olson, former legislative counsel to Senator Bill Frist. The comment was made by Dean Rosen, health policy adviser to the senator. Rolling Stone and Salon.com regret the error. 

    Kennedy Report Sparks Controversy 

    “Deadly Immunity,” our story about the link between mercury in vaccines and the dramatic rise in autism among children [RS 977/978], sparked intense reaction from the medical establishment and several leading news organizations. The story, by Robert F. Kennedy Jr. — part of an ongoing collaboration with Salon.com — documented the government’s efforts to conceal alarming data about the dangers of vaccines. 

    What is most striking is the lengths to which major media outlets have gone to disparage the story and to calm public fears — even in the face of the questionable science on the subject. In a segment on World News Tonight titled “A Closer Look,” ABC pointed out that Kennedy is “not a scientist or a doctor” and dismissed his extensive evidence as nothing more than “a few scientific studies.” The network also trotted out its medical editor, Dr. Timothy Johnson, to praise the “impeccably impartial Institute of Medicine” and to again state that Kennedy is not a scientist. 

    The New York Times, in a front-page story on the subject, devoted only one line to Kennedy’s article, which it said accused public-health officials and drugmakers of “conspiring” to hide the data on autism — a word that our story neither used nor implied. (The Wall Street Journal, in an op-ed attacking the article, was even more misleading, using the word “conspiracy” four times.) The Times then went on, for more than a full page, to portray concerns over vaccines as nothing more than the misguided fears of parents who suffer from “scientific illiteracy,” unable to understand the medical studies that prove immunizations to be safe. It depicted studies reviewed by the Institute of Medicine as definitive without even bothering to address the host of serious questions raised about their validity: conflicting diagnoses of autism, mixed-up data from HMOs and research skewed to exclude many sick kids. 

    Rolling Stone and Salon fact-checked the article thoroughly before publication, insisting on primary documentation for every statement in the story, and posted links to the most significant materials online to enable readers to judge for themselves. The final article contained six errors. These ranged from inadvertently transposing a quote and confusing a drug license for a patent to relying on a figure that incorrectly calculated an infant’s exposure to mercury over six months, rather than citing the even more dangerous amount injected on a single day. (The mistakes were corrected online as soon as they were discovered and can be viewed in detail at both RollingStone.com and Salon.com.) 

    It is important to note, however, that none of the mistakes weaken the primary point of the story. The government’s own records show that it has failed to do the science necessary to put to rest reasonable concerns about vaccines. If the scientists had simply done their job rather than covering their tracks, there would be no controversy today. Instead, the government cannot even provide a definitive figure of the number of cases of autism among American children — a number obviously critical to any serious scientific investigation — and yet expects the public to believe that it has ruled out any link between vaccines and an illness it does not even track. 

    “Science,” as one doctor in our story insisted, “is best left to scientists.” But when the scientists fail to do their job, resorting to closed-door meetings and rigged studies, others in society have not only a right but a moral obligation to question their work. In the coming years, further research may indeed demonstrate that mercury in vaccines is not responsible for the rise in autism. For now, though, we can only raise a very real and legitimate alarm — and hope that the government’s well-documented mishandling of its own research did not needlessly jeopardize the health of hundreds of thousands of children.

    Jul 232009
     

    CONTENTS 

    (1)  ADRIANE CARR, SASKATOON-REGINA, AUG 5-6 (WED-THUR) ON NUCLEAR 

    (2)  CANADA-U.S. WESTERN ENERGY CORRIDOR DOESN’T SAY …

    (3)  LEAD-UP TO INTERNATIONAL CLIMATE CHANGE MEETING IN COPENHAGEN IN DECEMBER

     (4)  BRUCE POWER WITHDRAWS APPLICATIONS FOR NEW BUILD (BRUCE C AND NANTICOKE) IN ONTARIO 

    (5)  NUCLEAR ENERGY THREATENS ONTARIO’S GREEN FUTURE.  COST OF NEW NUCLEAR REACTORS FOR DARLINGTON ESCALATES TO $26 BILLION.

    Note:  There is news such as #4 & #5 coming out every day. I took these from Elaine Hughes’ Stop the Hogs, NUKE NEWS. Contact her [tybach AT sasktel.net] to subscribe, if you want a news feed that is strictly nuclear. There are high quality feeds, and it’s all provided by volunteers, at no cost. We cross-feed. /Sandra 

     ============ 

    (1)  ADRIANE CARR, SPEAKING ON NUCLEAR IN SASKATOON & REGINA, AUG 5-6, WED-THUR

    On the energy issue, the Green Party has always been firmly in favor of investment in conservation, renewables, and demand-side management.  Nuclear is extremely expensive among other things, and not the way to go. 

    But hear what the Federal Deputy Leader has to say!  Adriane Carr will explain the Green Party policy on the nuclear question at meetings in Saskatoon and Regina.

    Adriane is pretty amazing, working for the public good with her husband Paul, for three decades.  People in B.C. where she was the leader of the B.C. Greens before moving into the federal arena, know her best.  She is a close personal friend and supporter of Elizabeth May.

    Wikipedia has good biographical information:  http://en.wikipedia.org/wiki/Adriane_Carr  

     This is a great opportunity to meet Adriane (and Paul) in person (if you’re in Saskatchewan!). 

    From Deputy Leader, Green Party of Canada, Adriane Carr:

    Hi Sandra – that’s a great schedule of activities!

    I’ll aim to be in Saskatoon by 2 pm on Wednesday August 5th. I can take media calls prior to that.

    I’d like to do some canvassing. If there are nominated candidates, I’d also like to do some street canvassing to collect signatures on their nomination papers. I’m quite comfortable talking on the nuclear energy/uranium issue. I was part of the campaigns to stop uranium mining in BC since the early 1980s.

    Yours,

    Adriane

    (deleted section)

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

    (2)  CANADA-U.S. WESTERN ENERGY CORRIDOR DOESN’T SAY … 

    The following might be helpful to some of you. I used it as a hand-out at a couple of public events.  It’s important to understand the “why” behind the nuclear agenda.  And the consequences – not just the financial ones (huge public debt). If you’d like the word document, please ask – it’s formatted!

    ————–

     First, thanks on behalf of everyone to Cathy for her insights: 

    Hi Sandra

     some quick comments. 

    “a lot of money to be made” – I don’t know if that is really true. I think a more likely scenario is that nuclear will be heavily subsidized by the taxpayer and it will not be profitable. The company would operate like a P3 – with a guaranteed floor price, excess costs to be paid out of the public purse. This is in fact what Bruce Power has set up with the Ontario government. See page 7 of Cameco Corporation Management’s Discussion and Analysis (MD&A) For the period ended March 31, 2009: 

    – 7 –

    BPLP’s Outlook for 2009

    Electricity revenue in 2009 is expected to decrease 5% to 10% over 2008 due to lower realized electricity prices compared to the 2% to 5% increase previously reported. Reduced industrial demand coupled with expanding supply and lower fossil fuel prices is expected to negatively impact electricity prices in Ontario for the remainder of 2009.

    (EMPHASIZE)  However, output from the B reactors is protected by a floor price.

     Therefore, in 2009 BPLP expects to receive significant support payments from the province of Ontario under the BPLP restructuring agreement. These payments can be used to fund ongoing operations and obligations and are subject to repayment in future years in the event electricity prices increase and remain above the floor price. As a result, support payments are considered a source of financing and not revenue or cash provided by operations.  (emphasis added). 

    This report is available from the SEDAR website.

     I think this distinction is strategically important. Business people often consider anything that makes money to be a good idea. If it makes money for someone there will be gravy to spread around … However if it is just going to raise taxes they will be less likely to support it. 

    There is also the general “market mentality” out there that if it makes money it must be doing something right, serving a need, etc. So I think it is dangerous to assume a profit motive for the nuclear industry in the old-fashioned business sense of the word. I think they are after spoils of the tar sands industry, both in terms of public money and power.

     Second – the “green argument” – can be tricky. If you assume that the tar sands will be developed no matter what, there is an argument (boo) for using nuclear instead of natural gas for providing heat. Some people will be willing to say that we cannot get “off” oil, there is no way to stop tar sands, so let’s at least not burn up all our natural gas in the process. I think the conservation message, coupled with a quality of life message (are people happier now that they are commuting more? etc.) needs to be front and centre.

     Related to that, I think the GHG emissions of the oil and gas industry need to be separated from “residential/domestic” use in Saskatchewan. We get shamed by the stats that our per capita emissions are among the highest in the world – yet much of those emissions are due to poor regulation and enforcement of standards in oil and gas production – something as citizens we can do nothing about unless we can force the government to put in better policies.

    Cathy

    NOTE:  See Item 4, just received from Elaine Hughes re Bruce Power not going to build two new reactors in Ontario – reinforces statements regarding reduced demand in Ontario.

     —————               

    The “largest on the planet” Canada-U.S. Western Energy Corridor, “spearheaded” by Brad Wall  

    Saskatoon Star Phoenix, June 15th, 2009  Page D8.  Originated in Calgary Herald.  Also ran in Vancouver Sun. 

    The article does not mention: 

    a.    The symbiotic relationship between the oil companies (tar sands) and the nuclear reactor industry.

    Natural gas supplies used in tar sands development are running out.  Nuclear reactors are required to provide the heat source for tar sands expansion.  The two industries enable profitability for each other.

    b.    There is a lot of money to be made by a few people (at public expense of building, maintaining, de-commissioning, transmission lines, environmental and health costs, etc) if private interests can sell electricity for tar sands expansion.

    But there is also a large and profitable market for electricity in the U.S. (again, if the public purse pays costs – public debt).  There is a 50/50 chance that hydro-electric power generation at the Hoover and Glen Canyon Dams will disappear by 2017 because of steadily declining water levels – a water and an electricity crisis in the western U.S..  (Feb 2008 Report by the Scripps Institution of Oceanography (University of California in San Diego).  A private consortium (MATL) is trying to build a high power transmission line from Lethbridge south into Montana.  Citizens are appealing through the court system to stop it.

     c.    Just the EXISTING sulphur dioxide and nitrous oxide emissions (acid rain) from tar sands production have put areas in northern Saskatchewan past critical load limits.  The plans for tar sands expansion will kill the north, just as for example, Ogoni lands in Nigeria have been destroyed by the oil companies.

     d.    The wisdom (?) of addressing the looming water (electricity) crisis in the U.S. by drawing down our own water supply.  Tar sands and nuclear production both place extra strains on our water supply, when the Rosenberg Report advises against extra loads on prairie water supplies.  The glaciers are melting;  climate-change models put the reduction in run-off in the range of 10 – 30% per year. 

     e.    The moral issue:  building nuclear reactors to expand tar sands production.  Saskatchewan’s per capita greenhouse gas emissions are among the highest on the planet.  Do we have moral obligations? (Cathy’s note ” We get shamed by the stats that our per capita emissions are among the highest in the world – yet much of those emissions are due to poor regulation and enforcement of standards in oil and gas production – something as citizens we can do nothing about unless we can force the government to put in better policies.” – Enforced Regulations.)

     f.    The beneficiaries of the destruction in Saskatchewan will be large corporate private interests.  Bruce Power means the electricity supply in Saskatchewan will have been privatized.

    Lessons from history:  California Electricity Crisis, Governor Gray Davis, 2001 State of the State address. “California’s deregulation scheme is a colossal and dangerous failure.  It has not lowered consumer prices.  And it has not increased supply.  In fact, it has resulted in skyrocketing prices, price-gouging, and an unreliable supply of electricity.  In short, an energy nightmare . . .  we have lost control over our own power.  We have surrendered the decisions about where electricity is sold –  and for how much –  to private companies with only one objective:  maximizing unheard-of profits.” 

    g.    Bill Boyd, Sask Minister responsible for the uranium/nuclear development, ties the “Energy Council” (legislators and energy industry representatives) to the Western Energy Corridor and to the UDP Report.  These matters are not discussed with the public and in the Legislature, but in closed meetings with industry. 

    The SANE choice of:

    –     Conservation and demand-side management

    –     Investment in the transition to alternatives

    would put us in a league with progressive jurisdictions. 

    We cannot grow more water for the Colorado River so it can generate electricity,  we cannot grow more water for the North Saskatchewan River.   We cannot grow more cheap oil or even more dirty tar sands – they aren’t renewable sources.   We seem unable to grasp the fact that the future lies somewhere else. 

    Because our economy is dependent upon CHEAP oil, the route that uses nuclear energy to fuel tar sands development, that DENIES we have a problem with our energy source (it’s running out), will only ensure that we have more and repeated economic crisis, in a downward and very destructive spiral.   Surely that is evident from the current economic crisis.  When the price of oil runs up to $150 a barrel, it sends shock-waves through an economy built upon $50 a barrel oil. 

     Conservation and renewables.  There is no place for expensive detours into nuclear energy that only serve to enable more “over fishing”.  We need to invest in TRANSITION OFF hydro-carbons.

     Dictionary for euphemisms in the following newspaper article:

    “Non-renewable “ = tar sands options

    “Clean-energy” = nuclear energy 

    – – – – – – – – – – –

     THE NEWSPAPER ARTICLE

     Premiers, governors, promote Canada-U.S. energy corridor   –  HYPERLINK  to June 15, 2009

    =================== 

     (3)  LEAD-UP TO INTERNATIONAL CLIMATE CHANGE MEETING IN COPENHAGEN IN DECEMBER

     All the Canadian Premiers are meeting in Regina in August. National groups will be there, under the umbrella Climate Action Network, to exert pressure on Canadian officials to TRANSITION OFF HYDRO-CARBONS.  We (Canadians) want to do our part in the global effort to mitigate against climate change.  

    PLEASE LET PEOPLE KNOW ABOUT THE EVENTS IN REGINA, AUGUST 5 TO 7. (scroll down) WARM BODIES ARE NEEDED!  YOU ARE GUARANTEED TO HAVE FUN IN THE PROCESS~! 

    —————

     July 30 – August 9th.  People will be spreading the word at the Saskatoon Fringe Festival – about Rally and Parade —  SEE Sunday October 4th. 

    —————

     July 31st:  deadline for public input to UDP (Uranium Development Partnership) public consultation (Chair: Dan Perrins). Very important.  If the Sask Government proceeds with the recommendations in the UDP Report, nuclear energy will be used to fuel expansion of the tar sands – it will be a kiss of death to efforts to address climate change.  Details for making a submission to Dan Perrins are in an email I’ll send later.

     ————— 

    August 5-7 Regina:  the COUNCIL OF THE FEDERATION (the meeting of the provincial premiers), Government House.

     —————

     August 5-7 Regina:  The CLIMATE ACTION NETWORK (CANet) is coordinating and organizing events. Groups include Clean Green Regina, Greenpeace, Sierra Club, Federation of Labour, Council of Canadians, Pedal for the Environment (cyclist group to arrive before the Federation mtg), SES (Sask Environmental Society) and Oxfam. 

    Tuesday August 4 – film night

    Aug 5  – teach-in and workshops

    Aug 6 – a rally at noon at the Legislature.

     August 6th  Pedal for the Planet  (GreenPeace initiative) http://kyotoplus.ca/pedal/?page_id=113

     ————— 

    August  5, Wednesday, 7:30 pm  Saskatoon: 

    MAYFAIR UNITED CHURCH, 902-33rd St. West.  Adriane Carr Deputy Leader Green Party of Canada, speaks on nuclear issue. 

    —————

    August 6, Thursday, 7:30 pm Regina:

    UNITARIAN CENTRE, corner of College Ave. and Angus St – 2700 College Ave.  Adriane Carr Speaks on Nuclear Energy

    —————

    August 6, Thursday,  7:30,  Frances Morrison Public Library Saskatoon:    The Saskatoon Peace Coalition is sponsoring the film “The Strangest Dream”.  Michael Murphy from the Saskatoon Peace Coalition will introduce Mayor Don Atchison who will give greetings from the City of Saskatoon  You can read about it at

    http://www3.nfb.ca/webextension/strangest-dream/synopsis.php

    —————

    August 9th, 12-4:00 St Joseph’s Church Hall (Broadway & 8th Street) Saskatoon:   Nagasaki Day event.  Our 15 minute slot (no nukes) is toward the end of the afternoon. We will have a table with info. 

    —————

    August 12 Pedal for the Planet in Saskatoon

    —————

    August 31:  UDP (Uranium Development Partnership) public consultation (Chair: Dan Perrins) report due.  Government will take a bit of time before responding.

    —————

    September 16-17 :  Nuclear Waste Management Organization (NWMO)  meeting in Saskatoon (believed to be at the Bessborough Hotel)

    The meeting is about the siting of radioactive waste disposal for the whole continent, in northern Saskatchewan.

    ” The discussion document about the proposed site selection process is on www.nwmo.ca. Click on “What’s new” and you’ll find “Invitation to Review a Proposed Process for Selecting a Site”.  They are asking for public comments.

    Ann

    Ann Coxworth

    Research Advisor

    Saskatchewan Environmental Society”

     The NWMO says that the decision is up to an individual selected (poor, First Nations) community; the decision is not up to the people of the province (the Government).  Richard Florizone repeated that idea in the video-taped presentation that was shown to the Saskatchewan public during the public consultations on the UDP Report.  Saying things doesn’t make them true.

     After drilling a test hole, Manitoba passed a law a number of years ago.  They will not receive radioactive waste from other jurisdictions in Manitoba.

     The industry has been creating radioactive waste for 50 years, without any idea of how to dispose of it.  At the very least, as a minimum requirement, they must STOP producing radioactive waste until they know where it is going to go.

     —————

     Sept 19 or 26  Saturday. Tentative.  Swift Current (Brad Wall’s constituency) RALLY:  anti-nuke pro-renewable rally at constituency office.  Locally organized.

     —————

     Sept 23:  Regina  Dr. Dale Dewar speaks on The Effect of Radiation on Humans. (Clean Green Regina)

     —————

     Sept 26 Saturday Swift Current:  KAIROS (Ecumenical Church group) Annual Meeting with representatives from Alberta and national office, etc.  Prairie region of KAIROS is ally in anti-nuke pro-renewable struggle.

     —————

     PROVINCIAL BY-ELECTIONS (Regina & Saskatoon) AROUND THIS TIME, OR IN NOVEMBER

     —————

     Oct 4 Sunday, 1:00 pm in Saskatoon   Provincial RALLY AND PARADE: “no-nuke, go-renewable”

     —————

     MUNICIPAL ELECTIONS IN THIS TIME PERIOD

     —————

     Oct 22, Regina:  opening day of the Legislature.   Rally on the steps of the Legislature.  What does the Speech from the Throne say about nuclear issue?  “no-nuke, go-renewable”?  OR this event will be in concert with Oct 24. 

     —————

     Oct 24 – Global Day of Climate Action.  international efforts being made to support this event (SES, Oxfam working on it.) www.350.org     

     —————

     PROVINCIAL BY-ELECTIONS (Regina & Saskatoon) AROUND THIS TIME, IF NOT IN EARLY FALL

     —————

     December 2009, the next UN Climate Change Conference, in Copenhagen

     =====================

     (4)  BRUCE POWER WITHDRAWS APPLICATIONS FOR NEW BUILD (BRUCE C AND NANTICOKE IN ONTARIO 

     From: Gordon Edwards

    Sent: Thursday, July 23, 2009 9:59 AM

    Background: 

    Earlier, Bruce Power submitted applications to build two new reactors (each 2200 MW) at its Bruce site on Lake Huron, and also another reactor (2200 MW) at the Nanticoke site on Lake Ontario. 

    In the last four years, electricity demand in the province of Ontario has been falling — to the extent that Ontario was paying clients to take the surplus electricity.  Hydropower had to be “wasted” to keep the nuclear plants running, and finally even the nuclear plants had to start being shut down due to lack of demand (Unit 8 of the Bruce B plant, 800 MW, was shut down July 17 due to lack of demand — only the second time in the history of the plant that this step has been taken.  The first time was one month earlier for similar reasons.).

     At the end of June, the government of Ontario announced that it has postponed its decision to buy new reactors because of the excessive price attached to the new build proposals.

     Gordon Edwards.

     ———–

     Bruce Power to Focus on Additional Refurbishments at Bruce A AND B

     http://www.earthtimes.org/articles/show/bruce-power-to-focus-on,902128.shtml

     Bruce C and Nanticoke new build applications withdrawn

     MARKETWIRE

     TIVERTON, ON – July 23, 2009 – Bruce Power will focus on the refurbishment of its remaining Bruce A and B units rather than build new reactors in Bruce County in order to supply Ontario with 6,300 megawatts of electricity.

     Bruce Power will also withdraw its application to build new reactors in Nanticoke given Ontario’s declining electricity demand. This has no impact on the current process to introduce nuclear energy to either Alberta or Saskatchewan, where both provincial governments are expected to release policy statements regarding nuclear’s role later this year.

     “These are business decisions unique to Ontario and reflect the current realities of the market,” said Duncan Hawthorne, Bruce Power’s President and Chief Executive Officer. “Our focus has always been to find the best way to provide Ontario with a long-term supply of 6,300 megawatts. For more than five years, we’ve examined our options and refurbishing our existing units has emerged as the most economical.” 

    Bruce Power has notified the Canadian Nuclear Safety Commission and the Canadian Environmental Assessment Agency that it will withdraw its site license applications and suspend its Environmental Assessments in Bruce County and Nanticoke.

    It will now work with its investors and the Ontario Power Authority to investigate the feasibility of refurbishing Units 3-8 following the successful restart of Units 1 and 2, which will inject another 1,500 MW of baseload generation into the Ontario market.

    For Bruce Power, refurbishing its remaining units could create up to 3,000 construction jobs and represent a multi-billion dollar investment over the next 10 years. It would also secure the long-term employment of up to 4,000 people to operate the site’s eight units over their extended lives.

     “While we have chosen to pursue the refurbishment option, I want to thank everyone in Bruce, Haldimand and Norfolk counties who supported us,” Hawthorne said. “The work we have done confirmed both sites held great promise for new build if the market conditions were more favourable. However, the time has come to narrow our focus and follow the route that’s best for us, for Ontario and its ratepayers.” 

    About Bruce Power

    Bruce Power is a partnership among Cameco Corporation, TransCanada Corporation, and BPC Generation Infrastructure Trust — a trust established by the Ontario Municipal Employees Retirement System, the Power Workers’ Union and The Society of Energy Professionals.

     For further information, please contact: Steve Cannon 519-361-6559 steve.cannon  AT  brucepower.com

    24-hour Duty Media Officer 519-361-6161

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

     (5)  NUCLEAR ENERGY THREATENS ONTARIO’S GREEN FUTURE.  COST OF NEW NUCLEAR REACTORS FOR DARLINGTON ESCALATES TO $26 BILLION.

    Nuclear energy threatens Ontario’s green future

    http://www.greenpeace.org/canada/en/recent/nuclear-costs-revealed

     We won’t say we told you so to Ontario Energy Minister George Smitherman about skyrocketing costs for nuclear plants, but we should. A news story this week revealed that the cost of new nuclear plants for the Darlington site near Toronto has escalated to $26 billion from an initial government estimate of $6 billion.

     Greenpeace nuclear campaigner Shawn-Patrick Stensil has been telling the government this for months.

     Find out what else Greenpeace knows about energy in Ontario.

    Read letter from Greenpeace and other enviro groups to Premier Dalton McGuinty. 

    Read a backgrounder on green energy vs. nuclear energy in Ontario.

    Take action now.  (click on their web-site)

    Jul 012009
     
    March 2012 update – – see  http://sandrafinley.ca/?p=4829
    = = = = = = = =
    NATIONAL SECURITY AGENCY (NSA)    
    SECOND OF TWO REPORTS ON THE DATA CENTRE
    The National Security Agency is planning to build a $1.6 billion storage facility in Utah to warehouse personal data.  (UPDATE:  it got bigger).   The giant facility will contain more than 1 million square feet of data center space. Construction is scheduled to begin in June 2010 and be completed by March 2013. The new facility is estimated to require as much electricity as all of  Salt Lake City. All forms of electronic data will be stored at the center, such as intercepted phone calls, e-mail messages, Internet searches and other communications intercepted by the agency.
    The effort was publicly disclosed in early 2008 and is designed to bolster cybersecurity-related awareness and incident response across the federal government. Much of the effort remains highly classified. It is partly an effort by federal agencies to reduce their exposure to Internet-based threats by reducing and consolidating the number of external Internet connections across government.  Instead of having each agency manage its own Internet connections, the plan involves having a small group of  Trusted Internet Connection (TIC) providers administer centralized connectivity and gateway-monitoring services for federal agencies. Critics of the project argue that the collection and permanant storage of such personal data is not necessary for national security purposes and intrudes upon the privacy rights of citizens.
    = = = = = = = = = = = = = = = = = = = = = = = =  ==
    FIRST OF TWO REPORTS ON THE DATA CENTRE

    NSA Plans $1.6 Billion Utah Data Center

    July 1st, 2009 : Rich Miller The National Security Agency is planning to build a massive data center at Fort Williams in Utah, which could eventually include more than 1 million square feet of data center space, reports the Salt Lake Tribune.
    The first phase of the project will feature an $800 million investment in a 35-megawatt data center, with a second $800 million, 35-megawatt phase to follow. The initial phase is currently in the design stage, with construction scheduled to begin in June 2010 and be completed by March 2013, according to documents (link via Mark Fontecchio). Project specs call for a Tier III raised-floor facility.
    The Utah project was enabled by a new funding bill signed last week by President Obama, which also provides money for an expansion of the power infrastructure at Fort Meade, Maryland where the NSA’s primary data center is located. The NSA’s operations at Fort Meade have reportedly been power-strapped since 2006, when the agency maxed out the electric capacity of the Baltimore Gas & Electric power grid.
    The NSA facility will be the third huge data center to be built in Utah, which has prevailed in several of the most competitive data center projects in the Western U.S. In May 2008 Oracle Corp. (ORCL) said it would build a $285 million data center in West Jordan. In December West Jordan was also selected as the site for a $334 million eBay data center.
    Between them, the three projects represent more than $2.2 billion in data center investment in the state of Utah.