Monday, March 30, 2009
Google Tech Talk Gerd Leonhard on The Future (Video)
Gerd Leonhard is a Music & Media Futurist, Author, Speaker, Advisor, and Digital Media Entrepreneur. The Wall Street Journal calls Gerd one of the leading media futurists in the world. He is the Co-Author of the influential book "The Future of Music" (2005, Berklee Press), as well as the author of "Music2.0" (released 2/2008 www.music20book.com), and of "Open is King - The Future of Media beyond Control" (late 2008).
New Legislation Authorizes FEMA Camps In U.S.
A new bill introduced in Congress authorizes the Department of Homeland Security to set up a network of FEMA camp facilities to be used to house U.S. citizens in the event of a national emergency.
The National Emergency Centers Act or HR 645 mandates the establishment of “national emergency centers” to be located on military installations for the purpose of to providing “temporary housing, medical, and humanitarian assistance to individuals and families dislocated due to an emergency or major disaster,” according to the bill.
The legislation also states that the camps will be used to “provide centralized locations to improve the coordination of preparedness, response, and recovery efforts of government, private, and not-for-profit entities and faith-based organizations”.
Ominously, the bill also states that the camps can be used to “meet other appropriate needs, as determined by the Secretary of Homeland Security,” an open ended mandate which many fear could mean the forced detention of American citizens in the event of widespread rioting after a national emergency or total economic collapse.
Many credible forecasters have predicted riots and rebellions in America that will dwarf those already witnessed in countries like Iceland and Greece.
With active duty military personnel already being stationed inside the U.S. under Northcom, partly for purposes of “crowd control,” fears that Americans could be incarcerated in detainment camps are all too real.
The bill mandates that six separate facilities be established in different Federal Emergency Management Agency Regions (FEMA) throughout the country.
The camps will double up as “command and control” centers that will also house a “24/7 operations watch center” as well as training facilities for Federal, State, and local first responders.
The bill also contains language that will authorize camps to be established within closed or already operating military bases around the country.
As we have previously highlighted, in early 2006 Halliburton subsidiary Kellogg, Brown and Root was awarded a $385 million dollar contract by Homeland Security to construct detention and processing facilities in the event of a national emergency.
The language of the preamble to the agreement veils the program with talk of temporary migrant holding centers, but it is made clear that the camps would also be used “as the development of a plan to react to a national emergency.”
As far back as 2002, FEMA sought bids from major real estate and engineering firms to construct giant internment facilities in the case of a chemical, biological or nuclear attack or a natural disaster.
A much discussed and circulated report, the Pentagon’s Civilian Inmate Labor Program, was more recently updated and the revision details a “template for developing agreements” between the Army and corrections facilities for the use of civilian inmate labor on Army installations.”
Alex Jones has attended numerous military urban warfare training drills across the US where role players were used to simulate arresting American citizens and taking them to internment camps.
Read the new legislation in full below.
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National Emergency Centers Establishment Act (Introduced in House)
HR 645 IH
111th CONGRESS
1st Session
H. R. 645
To direct the Secretary of Homeland Security to establish national emergency centers on military installations.
IN THE HOUSE OF REPRESENTATIVES
January 22, 2009
Mr. HASTINGS of Florida introduced the following bill; which was referred to the Committee on Transportation and Infrastructure, and in addition to the Committee on Armed Services, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned
——————————————————————————–
A BILL
To direct the Secretary of Homeland Security to establish national emergency centers on military installations.
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the `National Emergency Centers Establishment Act’.
SEC. 2. ESTABLISHMENT OF NATIONAL EMERGENCY CENTERS.
(a) In General- In accordance with the requirements of this Act, the Secretary of Homeland Security shall establish not fewer than 6 national emergency centers on military installations.
(b) Purpose of National Emergency Centers- The purpose of a national emergency center shall be to use existing infrastructure–
(1) to provide temporary housing, medical, and humanitarian assistance to individuals and families dislocated due to an emergency or major disaster;
(2) to provide centralized locations for the purposes of training and ensuring the coordination of Federal, State, and local first responders;
(3) to provide centralized locations to improve the coordination of preparedness, response, and recovery efforts of government, private, and not-for-profit entities and faith-based organizations; and
(4) to meet other appropriate needs, as determined by the Secretary of Homeland Security.
SEC. 3. DESIGNATION OF MILITARY INSTALLATIONS AS NATIONAL EMERGENCY CENTERS.
(a) In General- Not later than 60 days after the date of the enactment of this Act, the Secretary of Homeland Security, in consultation with the Secretary of Defense, shall designate not fewer than 6 military installations as sites for the establishment of national emergency centers.
(b) Minimum Requirements- A site designated as a national emergency center shall be–
(1) capable of meeting for an extended period of time the housing, health, transportation, education, public works, humanitarian and other transition needs of a large number of individuals affected by an emergency or major disaster;
(2) environmentally safe and shall not pose a health risk to individuals who may use the center;
(3) capable of being scaled up or down to accommodate major disaster preparedness and response drills, operations, and procedures;
(4) capable of housing existing permanent structures necessary to meet training and first responders coordination requirements during nondisaster periods;
(5) capable of hosting the infrastructure necessary to rapidly adjust to temporary housing, medical, and humanitarian assistance needs;
(6) required to consist of a complete operations command center, including 2 state-of-the art command and control centers that will comprise a 24/7 operations watch center as follows:
(A) one of the command and control centers shall be in full ready mode; and
(B) the other shall be used daily for training; and
(7) easily accessible at all times and be able to facilitate handicapped and medical facilities, including during an emergency or major disaster.
(c) Location of National Emergency Centers- There shall be established not fewer than one national emergency center in each of the following areas:
(1) The area consisting of Federal Emergency Management Agency Regions I, II, and III.
(2) The area consisting of Federal Emergency Management Agency Region IV.
(3) The area consisting of Federal Emergency Management Agency Regions V and VII.
(4) The area consisting of Federal Emergency Management Agency Region VI.
(5) The area consisting of Federal Emergency Management Agency Regions VIII and X.
(6) The area consisting of Federal Emergency Management Agency Region IX.
(d) Preference for Designation of Closed Military Installations- Wherever possible, the Secretary of Homeland Security, in consultation with the Secretary of Defense, shall designate a closed military installation as a site for a national emergency center. If the Secretaries of Homeland Security and Defense jointly determine that there is not a sufficient number of closed military installations that meet the requirements of subsections (b) and (c), the Secretaries shall jointly designate portions of existing military installations other than closed military installations as national emergency centers.
(e) Transfer of Control of Closed Military Installations- If a closed military installation is designated as a national emergency center, not later than 180 days after the date of designation, the Secretary of Defense shall transfer to the Secretary of Homeland Security administrative jurisdiction over such closed military installation.
(f) Cooperative Agreement for Joint Use of Existing Military Installations- If an existing military installation other than a closed military installation is designated as a national emergency center, not later than 180 days after the date of designation, the Secretary of Homeland Security and the Secretary of Defense shall enter into a cooperative agreement to provide for the establishment of the national emergency center.
(g) Reports-
(1) PRELIMINARY REPORT- Not later than 90 days after the date of the enactment of this Act, the Secretary of Homeland Security, acting jointly with the Secretary of Defense, shall submit to Congress a report that contains for each designated site–
(A) an outline of the reasons why the site was selected;
(B) an outline of the need to construct, repair, or update any existing infrastructure at the site;
(C) an outline of the need to conduct any necessary environmental clean-up at the site;
(D) an outline of preliminary plans for the transfer of control of the site from the Secretary of Defense to the Secretary of Homeland Security, if necessary under subsection (e); and
(E) an outline of preliminary plans for entering into a cooperative agreement for the establishment of a national emergency center at the site, if necessary under subsection (f).
(2) UPDATE REPORT- Not later than 120 days after the date of the enactment of this Act, the Secretary of Homeland Security, acting jointly with the Secretary of Defense, shall submit to Congress a report that contains for each designated site–
(A) an update on the information contained in the report as required by paragraph (1);
(B) an outline of the progress made toward the transfer of control of the site, if necessary under subsection (e);
(C) an outline of the progress made toward entering a cooperative agreement for the establishment of a national emergency center at the site, if necessary under subsection (f); and
(D) recommendations regarding any authorizations and appropriations that may be necessary to provide for the establishment of a national emergency center at the site.
(3) FINAL REPORT- Not later than 1 year after the date of the enactment of this Act, the Secretary of Homeland Security, acting jointly with the Secretary of Defense, shall submit to Congress a report that contains for each designated site–
(A) finalized information detailing the transfer of control of the site, if necessary under subsection (e);
(B) the finalized cooperative agreement for the establishment of a national emergency center at the site, if necessary under subsection (f); and
(C) any additional information pertinent to the establishment of a national emergency center at the site.
(4) ADDITIONAL REPORTS- The Secretary of Homeland Security, acting jointly with the Secretary of Defense, may submit to Congress additional reports as necessary to provide updates on steps being taken to meet the requirements of this Act.
SEC. 4. LIMITATIONS ON STATUTORY CONSTRUCTION.
This Act does not affect–
(1) the authority of the Federal Government to provide emergency or major disaster assistance or to implement any disaster mitigation and response program, including any program authorized by the Robert T. Stafford Disaster Relief and Emergency Assistance Act (42 U.S.C. 5121 et seq.); or
(2) the authority of a State or local government to respond to an emergency.
SEC. 5. AUTHORIZATION OF APPROPRIATIONS.
There is authorized to be appropriated $180,000,000 for each of fiscal years 2009 and 2010 to carry out this Act. Such funds shall remain available until expended.
SEC. 6. DEFINITIONS.
In this Act, the following definitions apply:
(1) CLOSED MILITARY INSTALLATION- The term `closed military installation’ means a military installation, or portion thereof, approved for closure or realignment under the Defense Base Closure and Realignment Act of 1990 (part A of title XXIX of Public Law 101-510; 10 U.S.C. 2687 note) that meet all, or 2 out of the 3 following requirements:
(A) Is located in close proximity to a transportation corridor.
(B) Is located in a State with a high level or threat of disaster related activities.
(C) Is located near a major metropolitan center.
(2) EMERGENCY- The term `emergency’ has the meaning given such term in section 102 of the Robert T. Stafford Disaster Relief and Emergency Assistance Act (42 U.S.C. 5122).
(3) MAJOR DISASTER- The term `major disaster’ has the meaning given such term in section 102 of the Robert T. Stafford Disaster Relief and Emergency Assistance Act (42 U.S.C. 5122).
(4) MILITARY INSTALLATION- The term `military installation’ has the meaning given such term in section 2910 of the Defense Base Closure and Realignment Act of 1990 (part A of title XXIX of Public Law 101-510; 10 U.S.C. 2687 note).
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- Hurricane Gustav: National Emergency Environment Sets the Stage for the McCain Election Campaign
- NIST Concludes “Fire” Caused WTC 7 “Collapse” when FEMA Report Concluded Fuel Tank Explosion had “low probability” of Knocking Down Tower
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- Torture Camps Minutes From Olympic Sites
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- There Might Be a Financial Crisis, But the World’s Arms Dealers Are Doing Just Fine
Indigenous Native American Prophecy (Video)
The question is whether we will experience the same fate. Will the earth end up as a barren planet, razed to the ground by nuclear weapons, earthquakes, or floods? Has it happened before? Will it all happen again, as prophets have so often predicted? Or is there still hope for us all?
Healthy Eating: Artificial food additives affect children’s behavior
Research from a study of 297 children published in The Lancet found a significant number of children became more inattentive, impulsive and hyperactive when given a test drink with artificial additives. (The subjects were from the general population, not diagnosed with attention deficit hyperactivity disorder.) In England, where the study was conducted, people are calling for the additives to be banned from the food supply because the effects can lead to reading and other problems in school.
In the U.S., doctors are advising parents to check and possibly change their child’s diet before considering ADHD drugs.
In the February edition of The American Academy of Pediatrics Grand Rounds, two medical experts praised the current research and advised pediatricians to recommend ``a trial of preservative-free, food coloring-free diet'' when a child is hyperactive.
The connection between food additives and behavior was noted more than 30 years ago by an allergist, Ben Feingold. He also hypothesized certain children were sensitive to foods with salicylates, compounds similar to aspirin. He recommended trying an elimination diet and documented hundreds of case studies in which behavior improved.
Although rigorous research on the Feingold program is lacking, current research is substantiating many aspects of it. Fervent believers in Feingold’s methods support and manage the nonprofit Feingold Association. (www.feingold.org). In addition to salicylates, The Feingold Program recommends eliminating from the diet: all artificial (synthetic) colors, listed on the label as ``food coloring'', ``color added'' or by its FDA number, like FD&C Yellow #5 or FD&C Red #40 (both used in the Lancet study); artificial flavors listed as ``flavoring'' or ``artificial flavoring'' or artificial vanilla (vanillin); aspartame (an artificial sweetener); and three preservatives, BHA, BHT, and TBHQ – already removed from most food for children in the U.K.
Many children’s cereals contain BHT and artificial colors but Cheerios, Honey Nut Cheerios, Kashi, Barbara’s, and Trader Joe’s brands do not. Yogurts, like Stonyfield or Trader Joe’s, do not have artificial colors. Plain tortilla or potato chips trump artificially colored Doritos, barbeque potato chips or orange cheese curls. Choose clear Gatorade, Capri Sun Sport, or dilute natural juice (in half) with water for young athletes. Dye-free Motrin or Benadryl are also available now.
Related: It's Official: TV Linked to Attention Deficit Hyperactivity Disorder
The Truth Behind the Vaccine Cover-up
MSG Causes Most Obesity In US And Canada
Hidden Sources Of MSG In Foods
Sweet Misery: A Poisoned World
Aspartame - The Silent Killer
The Effects Of Fluoride On The Thyroid Gland
Fluoride & the Pineal Gland: Study Published in Caries Research
Psychiatry and the Schools: Mental Hygiene in the 21 st Century
Todays Children - Soldiers Of Tomorrow
Death from Ritalin - The Truth Behind ADHD
Vegan lifestyle good for the heart, body, soul and mind
Organic and vegan eating spawn good health, sustainable environment
Vegan lifestyle lessens effects of factory farms
British scientists to create synthetic blood
A major research project is to be announced this week that will culminate in three years with the first transfusions into human volunteers of "synthetic" blood made from the stem cells of spare IVF embryos. It could help to save the lives of anyone from victims of traffic accidents to soldiers on a battlefield by revolutionising the vital blood transfusion services, which have to rely on a network of human donors to provide a constant supply of fresh blood.
The multimillion-pound deal involving NHS Blood and Transplant, the Scottish National Blood Transfusion Service and the Wellcome Trust, the world's biggest medical research charity, means Britain will take centre stage in the global race to develop blood made from embryonic stem cells. The researchers will test human embryos left over from IVF treatment to find those that are genetically programmed to develop into the "O-negative" blood group, which is the universal donor group whose blood can be transfused into anyone without fear of tissue rejection.
This blood group is relatively rare, applicable to about 7 per cent of the population, but it could be produced in unlimited quantities from embryonic stem cells because of their ability to multiply indefinitely in the laboratory.
The aim is to stimulate embryonic stem cells to develop into mature, oxygen-carrying red blood cells for emergency transfusions. Such blood would have the benefit of not being at risk of being infected with viruses such as HIV and hepatitis, or the human form of "mad cow" disease. The military in particular needs a constant supply of fresh, universal donor blood for battlefield situations when normal supplies from donors can quickly run out.
But developing blood made from the cells of spare IVF embryos will raise difficult ethical issues for people not happy with the idea of destroying embryos to create stem cells. It also raises the intriguing philosophical question of whether the synthetic blood will have come from someone who never existed. In theory, just one embryo could meet the nation's needs.
The Wellcome Trust is believed to have promised £3m towards the cost of the project, with further funding coming from the blood transfusion services of Scotland, and England and Wales. The Irish government is also understood to be involved. A spokesman for the Wellcome Trust said complicated legal issues were still being ironed out between all the parties involved but that an announcement is likely to be made in the coming week.
The project will be led by Professor Marc Turner, of Edinburgh University, the director of the Scottish National Blood Transfusion Service. Professor Turner has been involved in studies investigating how to ensure donated blood is free of the infectious agent behind variant CJD, the human form of "mad cow" disease. Several vCJD patients are thought to have contracted the disease by blood transfusions.
Professor Turner was unavailable for comment but a spokeswoman for the National Blood Service for England and North Wales confirmed that negotiations on the joint research project were at an advanced stage and that legal, rather than scientific, issues were holding up the announcement.
The multi-centre collaboration is also understood to involve scientists at the Medical Research Council's Centre for Regenerative Medicine at the University of Edinburgh, and Roslin Cells, a spin-off company that has emerged out of the Roslin Institute, where Dolly the sheep was cloned in 1996.
Scientists in other countries, notably Sweden, France and Australia, are also known to be working on the development of synthetic blood from embryonic stem cells. And last year, a team from a US biotechnology company, Advanced Cell Technology, announced that it has been able to produce billions of functioning red blood cells from embryonic stem cells. But the US work had been held up because of funding problems dating back to the ban on embryonic stem cell work under the Bush administration. President Barack Obama has since reversed that policy.
In Britain, the project was held up because of the difficulty of finding funding for "translational" research that attempts to take scientific studies in the laboratory into the earliest stages of commercial development. This problem has now been overcome.
New Artificial DNA Points to Alien Life
CHICAGO — A strange, new genetic code a lot like that found in all terrestrial life is sitting in a beaker full of oily water in a laboratory in Florida, a scientist said today, calling it the first example of an artificial chemical system that is capable of Darwinian evolution.
The system is made of the four molecules that are the basic building blocks of our DNA along with eight synthetic modifications of them, said biochemist Steven A. Benner of the Foundation for Applied Molecular Evolution in Gainesville.
The main difference between the synthetic molecules and those that make up conventional DNA is that Benner's molecules cannot make copies of themselves, although that is just "a couple of years" away, he said.
The wild biochemistry finding, described to a small group of reporters today at the annual meeting of the American Association for the Advancement of Science, offers ideas about new types of life for scientists to look for beyond our planet, or even possibly hidden on our planet.
"Unless it happens to shoot at you with a ray gun, the life that you encounter off of Earth will not necessarily have same biochemistry as us," Benner said.
And the step from Benner's system to something that could be called artificial life is still large. "There is not enough information in them to build organisms," Benner said.
Expanded alphabet for DNA
For some 20 years, Benner's labs have been involved in trying to make artificial life or things approximating it, with similar genetic and inheritance properties to life on Earth. (Previously, Benner worked at the University of Florida.)
He and his colleagues have focused in part on expanding the DNA alphabet to develop an "Artificially Expanded Genetic Information System," which now has its own supporting molecular biology.
The building blocks of DNA are four chemicals called nucleotides that are referred to as A, C, T and G, for short. The nucleotides pair up and bond in predictable ways to form the double helix structure of DNA. Benner's new nucleotides, which he and his colleagues have named Z, P, V, J, Iso-C, Iso-G, X and K, are reshufflings of the constituents of those molecules found in our DNA.
The evolution in this system happens when the 12-letter genetic code makes copying mistakes and subsequent sequences have properties that make them more liable to get copied. Those sequences would survive in greater numbers than the original sequence.
Benner's synthetic approach was conceptualized using "ball and stick plastic model chemistry," he said, the technique used by James Watson and Francis Crick to arrive at the structure of the DNA molecule in 1953.
The human genome's DNA includes 3 billion base pairs. Some of the molecules synthesized in Benner's lab are 81 base pairs long — relatively short.
The molecules are "fed" and grow via a process called the polymerase chain reaction (PCR) that allows the molecules to make copies of themselves. Once the replication of the molecules in Benner's system is self-catalyzed, without PCR, the process is self-sustaining. Benner claims, "then it's artificial life."
Dreaming up extra-terrestrial life
The research resulted from a NASA-funded project to try to understand what life might look like beyond Earth. Such life might live in water, but it could also live in liquid nitrogen or methane (as speculated for Saturn's moon Titan) and in environments with extremely high or low acidity.
The results are published in a technical book, "Life, the Universe and the Scientific Method," of which Benner has made about 100 copies to distribute to his colleagues.
"One of the ways scientists try to understand life as a universal concept ... is you try to make life on your own in the lab," Benner said. "We try to put together chemicals that do that."
Any potential life forms made from such molecules would be "so alien in terms of their biochemistry that they will not able to eat you," Benner said.
NASA has been involved in searching for extra-terrestrial life along numerous avenues for decades, including the Viking mission to Mars in the 1970s and its recent missions to the red planet which have searched for signs of habitability there. NASA also funds an Astrobiology Institute, which partners with hundreds of researchers world-wide who study of the origins, evolution, distribution and future of life in the universe
The trick to searching for alien life is how to look for it, said Paul Davies of Arizona State University, who also spoke with reporters here today.
"All of the techniques which microbiologists use to [look for alien life] are customized to life as we know it," Davies said. "It's no surprise that microbiologists haven't come across micro-organisms that seem to have relatively different biochemistry."
In the future, more scientists could "talk with Steve Benner," Davies said, "to come up with perfectly good molecules that life could use — but doesn't."
Sunday, March 29, 2009
Barack Obama Born In Kenya? His Grandmother Says Yes.
Watch this interesting and important video clip.
I myself, not wanting to believe what I see, did some searching around, and this is what I came up with:
Obama was born on August 4, 1961, at the Kapiolani Medical Center.
and here it says:
Barack Obama was born at the Queen's Medical Center on 4 August 1961.
So which hospital was it, or was he really born in Kenya? And why is this simple matter so confusing and disturbing? Do the search your self and plug in these key words:
Obama born Queen's Medical Center and then Obama born Kapiolani Medical Center in a Google search. You will see he is reported to be born in two diferent hospitals. A miracle! Maybe he IS the Messiah (grin).
What's so hard about knowing something so simple as which hospital or country someone was born in? And if it is simple, then why doesn't Barack Hussein Obama just present the court with his original birth certificate to be analysed and proven? The onus of proof is on him, not the American public of which he wants their trust in him to be their leader.
So, who is lying? Barack? His grandmother? His sister? Someone is.
p.s. Dr. Jerome Corsi will be on my show today (Sunday) where I will be interviewing him about his recent trip to Kenya to promote his new book, The Obama Nation... * Dr. Corsi was not on my show Sunday, his publicist asked to re-schedule.
UFO files to be released under Obama Open Government Memoranda
On his first full day as President, Barack Obama issued two Executive Orders and three Presidential Memorandum that will start an era of transparent and Open Government. The White House Office of the Press Secretary released a statement outlining the sweeping changes to be implemented by the Obama administration. In his Presidential Memorandum on Transparency and Open Government, and the Presidential Memorandum on the Freedom of Information Act, President Obama instructed
... all members of his administration to operate under principles of openness, transparency and of engaging citizens with their government. To implement these principles and make them concrete, the Memorandum on Transparency instructs three senior officials to produce an Open Government Directive within 120 days directing specific actions to implement the principles in the Memorandum. And the Memorandum on FOIA instructs the Attorney General to in that same time period issue new guidelines to the government implementing those same principles of openness and transparency in the FOIA context.
President Obama emphasized that his Administration “is committed to creating an unprecedented level of openness in Government.” He furthermore said in a press conference announcing his Memoranda:
For a long time now, there's been too much secrecy in this city. The old rules said that if there was a defensible argument for not disclosing something to the American people, then it should not be disclosed. That era is now over. Starting today, every agency and department should know that this administration stands on the side not of those who seek to withhold information but those who seek to make it known.
Obama’s bold initiative for Open Government reflects the influence of the Co-Chair of his Presidential transition team, John Podesta. Podesta has long been an outspoken advocate of Open Government. On September 16, 2008, he gave a speech before the Senate Judiciary Subcommittee on the Constitution titled “Too Much Secrecy Puts Our Nation at Risk.”
Along with Leon Panetta, the new Director of the CIA, Podesta helped craft the Clinton Administration’s efforts to implement greater government openness through the passage of Executive Order 12958. Passed on April 17 1995, EO 12958 made it easier to declassify national security information that had been unnecessarily classified for decades. The Bush administration later neutralized key sections of EO 12958 thereby making it harder to declassify documents.
Less well known is that in October 22, 2002, Podesta petitioned for the release of UFO files that had been unnecessarily classified. He said: "I think it's time to open the books on questions that have remained in the dark on the question of government investigations of UFOs.”
John Podesta speaks about releasing UFO files at National Press Club
President Obama has decided to act quickly and decisively in instructing all adminstration officials to take action to implement principles of Open Government and Transparency. In the case of classified X-Files dealing with evidence of UFOs and extraterrestrial life, Obama’s Memoranda will make it easier for the release of such files in cases where national security is not compromised. The consequences of the release of X-Files of different government agencies and military departments will be momentous if they confirm that extraterrestrial life is visiting Earth.
The Two Best Ways To Download Music
step one go to google.com and type in "the artist - the album.rar"
sometimes i helps to put quotations around, sometimes it doesn't depending on where your searching
the artist and the album are examples like "agalloch the white.rar"
Often times the file wont we listed in a search engine but link to a blog that has links to the file will. There are also search engines that search upload sites like rapidshare megaupload, etc like http://www.uvrx.com/ http://www.megadownload.net/ http://www.shareminer.com/
.rar is the name of a file compression extension, like a zip file, but more common for albums to be compressed in one .rar file. In order to extract the folder and the mp3 album out of the .rar file you will need a application to extract .rar files. the best one that i know of would be winrar and it can be downloaded from that link. to unrar a file, install the software, then right click on a .rar file and extract it to a specified location.
The second way and more common way to download music is through torrents. this way is more popular as i sort of just invented the first way myself, but i'm sure other people have thought of it. .torrents are files that people upload/host and share through the internet. from computer to computer. randomly. the more seed there are on a torrent file the fast your download will be. if you download a torrent file that has very few seeds it could take a very long time or even never compete so its important to download from a file that has lots of seeds.
In order to download .torrent files you'll have to have a program unless you've heard of http://www.bitlet.com which will let you download .torrent files if you can copy and paste the link into the main box on the site and click enter and voila, your file starts downloading, with no software.
Software to download .torrent files is just as easy. got to bitcomet and download a copy of it and try it out. bitcomet will help you download .torrent files to your computer and once torrent files are done fully downloading they change into the extension that the file you downloaded was whether its .mp3 .avi , etc
You will have to search for sites that have links to .torrent files like thepiratebay , mininova , demonoid and from downloading torrents there they will be sent directly to bitcomet which automatically starts downloading the file, you dont have to download the file all at once and it can redownload from different computer start ups and still be the same file quality. with torrents you can search for just about anything from music to movies to software and games, whatever your into.
Simple And Easy Dr. Huadlas - Liver cleanse - Gallbladder cleanse - Liver flush
"Cleansing the liver of gallstones dramatically improves digestion, which is the basis of your whole health. You can expect your allergies to disappear, too, more with each cleanse you do! Incredibly, it also eliminates shoulder, upper arm, and upper back pain. You have more energy and increased sense of well being.
It is the job of the liver to make bile, 1 to 1.5 quarts in a day! The liver is full of tubes (biliary tubing) that deliver the bile to one large tube (the common bile duct). The gallbladder is attached to the common bile duct and acts as a storage reservoir. Eating fat or protein triggers the gallbladder to squeeze itself empty after about twenty minutes, and the stored bile finishes its trip down the common bile duct to the intestine.
For many persons, including children, the biliary tubing is choked with gallstones. Some develop allergies or hives but some have no symptoms. When the gallbladder is scanned or X-rayed nothing is seen. Typically, they are not in the gallbladder. Not only that, most are too small and not calcified, a prerequisite for visibility on an X-ray. There are over half a dozen varieties of gallstones, most of which have cholesterol crystals in them. They can be black, red, white, green or tan colored. The green ones get their color from being coated with bile. Notice in the picture (pg. 545) how many have imbedded unidentified objects. Are they fluke remains? Notice how man are shaped like corks with longitudinal grooves below the tops. We can visualize the blocked bile ducts from such shapes. Other stones are composites- made of many smaller ones- showing that they regrouped in the bile ducts some time after the last cleanse.
At the very center of each stone is found a clump of bacteria, according to scientists, suggesting a dead bit of parasite might have started the stone forming.
As the stones grow and become more numerous the back pressure on the liver causes it to make less bile. Imagine the situation if your garden hose had marbles in it. Much less water would flow, which in turn would decrease the ability of the hose to squirt out the marbles. With gallstones, much less cholesterol leaves the body, and cholesterol levels rise.
Gallstones, being porous, can pick up all the bacteria, cysts, viruses and parasites that are passing through the liver. In this way "nests" of infection are formed, forever supplying the body with fresh bacteria. No stomach infection such as ulcers or intestinal bloating can be cured permanently without removing these gallstones from the liver.
Preparation
- You can't clean a liver with living parasites in it. You won't get out many stones, and will feel quite sick. Zap daily the week before, or get through the first three weeks of the parasite killing program before attempting a liver cleanse. If you are on a parasite maintenance program, do a high dose program the week before.
- Completing the kidney cleanse before cleansing the liver is also recommended. You want your kidneys, bladder and urinary tract in top working condition so they can efficiently remove any undesirable substances incidentally absorbed from the intestine as the bile is being excreted.
- Do any dental work first, if possible. Your mouth should be metal free and bacteria free (cavitations are cleaned). A toxic mouth can put a heavy load on the liver, burdening it immediately after cleansing. Eliminate that problem first for best results.
Liver cleanse and gallbladder cleanse flush NO surgery
Ingredients
1/2 CupOlive Oil Extra Virgin (= 1.25 dl)
1 Big grapefruit (2 small) (Or 3 lemons)
4 tablespoon EPSOM salts = ( MgSO4 + 7H2O)
(EPSOM salts = Magnesium Sulphate = EPSOMITE = Magnesium Sulfate Heptahydrate)
3 cups water (=750 dl)
(P.S .!! 1 cup = 250 ml = 2.5 dl = 0.25 l )
[Comment inserted by webmaster:
You can substitute 3 cups water (=750 dl) (that is used in this recipe to dissolve Epsom salt) with 3 cups freshly pressed grapefruit juice, or freshly pressed apple juice . That way you will not feel unpleasant taste of Magnesium Sulphate
( = Magnesium Sulfate = Epsom salt = MgSO4 + 7H2O) ]
[If using lemon juice, do not blend juice with oil.
Drink little oil, little juice, from 2 differnt cups.
If you mix oil and juice, it may (it doesn't happens always) sligtly congell, and get a slimy consitence that is not easy to swallow.
It may become slimy.
It never happens with grapefruit juice!]
Choose a day like Saturday for the cleanse, since you will be able to rest the next day.
Take no medicines, vitamins or pills that you can do without; they could prevent success. Stop the parasite program and kidney herbs too, the day before.
Eat a no-fat breakfast and lunch such as cooked cereal with fruit, fruit juice, bread and preserves or honey (no butter or milk), baked potato or other vegetables with salt only. This allows the bile to build up and develop pressure in the liver. Higher pressure pushes out more stones.
2:00 PM. Do not eat or drink after 2 o'clock. If you break this rule you could feel quite ill later. Get your Epsom salts ready. Mix 4 tbs. in 3 cups water and pour this into a jar. This makes four servings, 3/4 (three fourths) cup each. Set the jar in the refrigerator to get ice cold (this is for convenience and taste only).
[ You can substitute 3 cups water with 3 cups freshly pressed grapefruit juice, or freshly pressed apple juice, it tastes better .]
6:00 PM. Drink one serving 3/4 (three fourths cup) of the ice cold Epsom salts. If you did not prepare this ahead of time, mix 1 tbs. in 3/4 (three fourth) cup water now. You may add 1/8 (one eight) tsp. vitamin C powder to improve the taste. You may also drink a few mouthfuls of water afterwards or rinse your mouth. Get the olive oil (ozonated, if possible) and grapefruit out to warm up.
Alternative Schedule 1: Omit the first Epsom Slats dose at 6 p.m. Take only one dose, waiting till 8 p.m. Change nothing else. Many people still get stones with one less dose. If you do not, do the full course next time. "The Cure For HIV and AIDS" By Hulda Clark pg.585
8:00 PM. Repeat by drinking another 3/4 (three fourths) cup of Epsom salts.You haven't eaten since two o'clock, but you won't feel hungry. Get your bedtime chores done. The timing is critical for success.
9:45 PM. Pour 1/2 (half) cup (measured) olive oil into the pint jar. Add 2 drops HCl to sterilize. Wash grapefruit twice in hot water and dry; squeeze by hand into the measuring cup. Remove pulp with fork. You should have at least 1/2 (half) cup, more (up to 3/4 (three fourths) cup) is best. You may use part lemonade. Add this to the olive oil. Also add Black Walnut Tincture. Close the jar tightly with the lid and shake hard until watery (only fresh grapefruit juice does this).
Now visit the bathroom one or more time, even if it makes you late for your ten o'clock drink. Don't be more than 15 minutes late. You will get fewer stones.
10:00 PM. Drink the potion you have mixed. Take 4 ornithine capsules with the first sips to make sure you will sleep through the night. Take 8 if you already suffer from insomnia. Drinking through a large plastic straw helps it go down easier. You may use oil and vinegar salad dressing, or straight honey to chase it down between sips. Have these ready in a tablespoon on the kitchen counter. Take it all to your bedside if you want, but drink it standing up. Get it down within 5 minutes (fifteen minutes for very elderly or weak persons).
Lie down immediately. You might fail to get stones out if you don't. The sooner you lie down the more stones you will get out. Be ready for bed ahead of time. Don't clean up the kitchen. As soon as the drink is down walk to your bed and lie down flat on your back with your head up high on the pillow. Try to think about what is happening in the liver. Try to keep perfectly still for at least 20 minutes. You may feel a train of stones traveling along the bile ducts like marbles. There is no pain because the bile duct valves are open (thank you Epsom salts!). Go to sleep, you may fail to get stones out if you don't.
Next morning. Upon awakening take your third dose of Epsom salts. If you have indigestion or nausea wait until it is gone before drinking the Epsom salts. You may go back to bed. Don't take this potion before 6:00 am.
2 Hours Later. Take your fourth (the last) dose of Epsom salts. You may go back to bed again.
"The Cure For HIV and AIDS" By Hulda Clark pg.585
Alternative Schedule 2: After taking the first dose of Epsom salts in the morning, wait two hours and take a second dose of the oil mixture (but only 1/2 cup)and go back to bed. After two more hours take another dose of Epsom salts. This schedule can increase the number of stones you remove."
After 2 More Hours you may eat. Start with fruit juice. Half an hour later eat fruit. One hour later you may eat regular food but keep it light. By supper you should feel recovered.
How well did you do?
Expect diarrhea in the morning.
Use a flashlight to look for gallstones in the toilet with the bowel movement.
Use colander to make sure you collect all stones
Look for the green kind since this is proof that they are genuine gallstones, not food residue. Only bile from the liver is pea green. The bowel movement sinks but gallstones float because of the cholesterol inside.
Calcified stones and stones containing protein may sink, but colander will catch all stones.
Count them all roughly, whether tan or green. You will need to total 2,000 stones before the liver is clean enough to rid you of allergies or bursitis or upper back pains permanently. The first cleanse may rid you of them for a few days, but as the stones from the rear travel forward, they give you the same symptoms again. You may repeat cleanses at two week intervals. Never cleanse when you are ill.
[HPS editors note: I started passing chaff through normal bowel movements after my 4th colon cleansing fast, approximately after a total of 4x14= 56 days of total colon cleansing within 9 months. The chaff continued in normal bowel movements for 8 months! Thousands of tiny stones, looked like small popcorn and small bee pollen granules, others looked like moth wings. Sometime I would drop at one bowel movement 50-100 pea size stones that would float in the water. It was truly an experience. Almost daily for 8 months! When I did my first Dr. Clark's liver cleanse I immediately dropped over 200 pea size green and tan stones, and when I examined them I was shocked. They crushed in my fingers and what I found was pure fat, pure cholesterol. Can you imagine hundred of them. Also in my second liver cleanse I had the same experience].
Sometimes, the bile ducts are full of cholesterol crystals that did not form into round stones. They appear as a "chaff" floating on top of the toilet bowl water. It may be tan colored, harboring millions of tiny white crystals. cleansing this chaff is just as important as purging the stones.
How safe is the liver cleanse? It is very safe. My opinion is based on over 500 cases, including many persons in their seventies and eighties. None went to the hospital; none even reported pain. However it can make you feel quite ill for one or two days afterwards, although in every one of these cases the maintenance parasite program had been neglected. This is why the instructions direct you to complete the parasite and kidney rinse program first.
This procedure contradicts many modern medical viewpoints. Gallstones are thought to be formed in the gallbladder, not the liver. They are though to be few, not thousands. They are not linked to pains other than gallbladder attacks. It is easy to understand why this thought: by the time you have acute pain attacks, some stones are in the gallbladder, are big enough and sufficiently calcified to see on X-ray, and have caused inflammation there. When the gallbladder is removed the acute attacks are gone, but the bursitis and other pains and digestive problems remain.
An excerpt from a message posted on CureZone Liver Flush Forums:Flush can remove some gallstones from some gallbladders
http://www.curezone.com/forums/fm.asp?i=1298598#i
Is there really any solid evidence that Gallstones can exit gallbladder?
If there was any solid evidence that Gallstones can exit gallbladder, why would any doctor claim that gallstones CAN NOT exit gallbladder?
Fact: Some gallstones (smaller gallstones) can exit gallbladder.
Fiction: All gallstones can exit gallbladder. Anyone believing that every stone can exit gallbladder is ignorant/uninformed or irrational. Rare stones can be even larger then 2 inch ( 5cm ) in smallest diameter.
Fiction: Gallstones can not exit gallbladder. Anyone believing that no stone can exit gallbladder is ignorant/uninformed or irrational. Stones can be smaller then 2 mm in diameter, and could easily travel through the bile ducts without any chance of causing obstruction.
Majority of gallstones starts their "life" as a microscopic crystal of cholesterol. Very few gallstones ever get a chance to grow larger then 2mm. Most are expelled while small as sand.
cholesterol = chole + sterol
The name originates from the Greek chole- (bile) and stereos (solid)
cholesterol = Greek for solid bile
How do we know that some gallstones can exit gallbladder?
It is a well documented medical phenomenon.
Obstruction of the common bile duct is often caused by gallstones that were expelled from the gallbladder:
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2407039&dopt=Abstract
In patients with chronic Pancreatitis, common bile duct obstruction is reported in 3.2-45.6% of patients; however, only 5-10% of all patients with chronic Pancreatitis require operative decompression of the bile duct.
http://www.virtualgastrocentre.com/diseases.asp?did=191
Passage of gallstones into the common bile duct occurs in approximately 10-15% of patients with Gallstones. The incidence is thus related to the presence of gallstones, which are very common (10-20% of population).
Common bile duct stone References
[1] Braunwald, Fauci, Kasper, Hauser, Longo, Jameson. Harrison's Principles of Internal Medicine. 15th Edition. McGraw-Hill. 2001.
[2] Cotran, Kumar, Collins 6th edition. Robbins Pathologic Basis of Disease. WB Saunders Company. 1999.
[3] Fletcher, D. Gallstones, In: Tjandra, JJ, Clunie GJ, Thomas, RJS (eds); Textbook of Surgery, 2nd Ed, Blackwell Science, Asia. 2001.
[4] Haslet C, Chiliers ER, Boon NA, Colledge NR. Principles and Practice of Medicine. Churchill Livingstone 2002.
[5] Hurst JW (Editor-in-chief). Medicine for the practicing physician. 4th edition Appleton and Lange 1996.
[6] Kumar P, Clark M. CLINICAL MEDICINE. WB Saunders 2002.
[7] Longmore M, Wilkinson I, Torok E. OXFORD HANDBOOK OF CLINICAL MEDICINE. Oxford Universtiy Press. 2001
[8] McLatchie G and LEaper DJ (editors). Oxford Handbook of Clinical Surgery 2nd Edition. Oxford University Press 2002.
[9] MEDLINE Plus
[10] Raftery AT Churchill's pocketbook of Surgery. Churchill Livingsone 2001.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1119388
Jaundice occurs in patients with gall stones when a stone migrates from the gall bladder into the common bile duct...
Acute pancreatitis
Acute pancreatitis develops in 5% of all patients with gall stones and is more common in patients with multiple small stones, a wide cystic duct, and a common channel between the common bile duct and pancreatic duct. Small stones passing down the common bile duct and through the papilla may temporarily obstruct the pancreatic duct or allow reflux of duodenal fluid or bile into the pancreatic duct resulting in acute pancreatitis.
Let us do some math here.
20% of people may develop gallstones during their life
15% of people with gallstones may experience obstruction of the common bile duct
How many people may experience obstruction of the common bile duct?
Answer: 3% of total population where 20% have gallstones.
What about USA?
Population of USA: 300 million.
How many people may experience obstruction of the common bile duct during their life?
3% = 9 million people in USA will experience obstruction of the common bile duct with gallstone(s), gallstone(s) that most likely was formed inside gallbladder, and then was expelled, only to be stuck into the common bile duct.
Question: Do all gallstones expelled from gallbladder end-up blocking common bile duct?
Answer: No, only gallstones that have specific size and/or shape.
By it's size and shape, the stone must be small enough or slim enough to pass through the cystic duct and exit gallbladder, but it should be large enough to stuck at the sphincter of oddi, and to block the flow of liquid bile and pancreatic juices into duodenum.
How many gallstones have that specific size and/or shape that would allow it to exit gallbladder, but would not allow it to pass through common bile duct or through the "sphincter of oddi"?
Nobody knows the answer to this question, of course.
But, we could estimate that less then 10% of all stones would qualify. That would be of course just an estimation.
We could estimate that 90% of gallstones (or gallbladder sand and sludge ) that exits gallbladder would not stuck in the common bile duct, and will never be registered. It would become feces.
What does that mean?
It could mean that majority of people with gallstones may have expelled some of their stones (or sand) at one time or another, without ever knowing it happened. Stones pass from bile ducts into intestines ... no pain ... no obstruction ... no symptoms ... no awareness .... nobody knows it happened. But it could be happening every day. That is what nature (evolution) intended for gallstones.
Remember that each stone starts as a microscopic crystal. Who could count the number of microscopic crystals that are existing gallbladder every day?
Why don't all stones pass?
Why don't gallbaldder get those crystals out before they become large enough?
There could be many reasons, like: the lack of phisical activity, poor diet, stress, dehydration, being owerweight, not drinking enough water, infection, illness, .... hundreds of oissible reasons.
What about USA?
Population of USA: 300 million.
Number of people who will develop gallstones: 20% = 60 million.
If 90% of them expel some smaller gallstones at one time or another during their life, then we have 54 million people who are going to pass or have already passed gallstones, and are not aware of it!!!
Estimation:
54 million of people in USA may expel some smaller gallstones from their gallbladder. 9 million people in USA will experience obstruction of the common bile duct, obstruction caused by a gallstone small enough to exit cystic duct, but too large to exit sphinscter of oddi..
The sphincter of oddi is situated in the upper intestine, or duodenum, at the site where the common bile duct enters intestine. Normally, this sphincter functions as a one-way valve to allow bile and pancreatic secretions to enter the bowel, while preventing the contents of the bowel from backing up into these ducts.
White Shark
ttp://www.curezone.com/forums/fm.asp?i=1298598#i
You can comment and debate this recipe on the Liver Flush Debate Forum here on CureZone.
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Liver cleanse & Gallbladder cleanse (Liver flush) (an alternative to gallbladder surgery)
Liver Cleanse FAQ
[Comment inserted by webmaster:
You can substitute 3 cups water (=750 dl) with 3 cups freshly pressed grapefruit juice, or freshly pressed apple juice that is used in this recipe to dissolve Epsom salt. That way you will not feel unpleasant taste of Magnesium Sulphate ( = Magnesium Sulfate = Epsom salt = MgSO4 + 7H2O) ]
Magnesium Sulfate used for liver cleanse
Chemical name: Magnesium Sulfate (Heptahydrate) or (Hydrated)
Chemical Formula: MgSO4 + 7H2O, Hydrated Magnesium Sulfate
Mineral: EPSOMITE (MgSO4 + 7H2O)
Other minerals: KIESERITE (MgSO4 + H2O, Hydrated Magnesium Sulfate)
Hexahydrite (MgSO4 + 6H2O)
MAGNESIUM SULFATE
Description
http://eilat.sci.brooklyn.cuny.edu/newnyc/drugs/magnesiu.htm
Magnesium sulfate reduces striated muscle contractions and blocks peripheral neuromuscular transmission by reducing acetylcholine release at the myoneural junction. In emergency care, magnesium
sulfate is used to manage seizures associated with toxemia of pregnancy. Other uses include uterine relaxation (to inhibit contractions of premature labor), as a bronchodilator after beta-agonist and anticholinergic agents have been used, replacement therapy for magnesium deficiency, as a cathartic to reduce the absorption of poisons from the Gl tract, and in the initial therapy for convulsions. Magnesium sulfate is gaining popularity as an initial treatment in the management of various dysrhythmias, particularly torsades de pointes, and dysrhythmias secondary to a tricyclic antidepressant overdose or digitalis toxicity. The drug is also considered as a class Ila agent (probably helpful) for refractory ventricular fibrillation and ventricular tachycardia after administration of lidocaine or bretylium doses.
===========================
Magnesium sulfate is effective for severe acute asthma treated in the emergency department
http://www.acponline.org/journals/ebm/sepoct99/rowe.htm
Intravenous magnesium sulfate reduces the rate of hospital admissions and improves pulmonary function in patients with severe acute asthma treated in the emergency department.
Sources of funding: Canadian Association of Emergency Physicians and National Institutes of Health.
============================
Magnesium sulfate is used to treat pre-eclampsia, eclampsia and preterm labor.
http://www.twinslist.org/magsulfate.html
Pre-eclampsia (also known as toxemia and Pregnancy-Induced High Blood Pressure) consists of high blood pressure, protein in the urine and edema (swelling). It can rapidly become severe pre-eclampsia, with very high blood pressure, visual disturbances, failing kidneys and elevated liver enzymes. In rare cases, pre-eclampsia develops into eclampsia, where potentially fatal convulsions occur. It also can become HELLP Syndrome (hemolysis (H), which is the breaking down of red blood cells, elevated liver enzymes (EL), and low platelet count (LP)), which is potentially fatal to both the woman and her baby or babies.
Also indexed as: L-ornithine-L-aspartate, Ornithine-aspartate, OA
What does it do?
Ornithine, an amino acid, is manufactured by the body when another amino acid, arginine, is metabolized during the production of urea (a constituent of urine). Animal research has suggested that ornithine, along with arginine, may promote muscle-building activity in the body by increasing levels of anabolic (growth-promoting) hormones such as insulin and growth hormone. However, most human research does not support these claims at reasonable intake levels.1 2 3 One study that did demonstrate increased growth hormone with oral ornithine used very high amounts (an average of 13 grams per day) and reported many gastrointestinal side effects.4 One controlled study reported greater increases in lean body mass and strength after five weeks of intensive strength training in athletes taking 1 gram per day each of arginine and ornithine compared to a group doing the exercise but taking placebo.5 These findings require independent confirmation.
In clinical studies on people hospitalized for surgery, generalized infections, cancer, trauma, or burns, supplementation with ornithine alpha-ketoglutarate has been reported to produce several beneficial effects.6 A double-blind trial evaluated the effects of ornithine alpha-ketoglutarate supplementation in elderly people recovering from acute illnesses;7 those who took 10 grams of ornithine alpha-ketoglutarate per day for two months had marked improvement in appetite, weight gain, and quality of life compared to those taking placebo. They also had shorter recovery periods and required fewer home visits by physicians and nurses and needed fewer medications.
Ornithine aspartate has been shown to be beneficial in people with hepatic encephalopathy (brain abnormalities) due to liver cirrhosis. In a double-blind trial, people with cirrhosis and hepatic encephalopathy received either 18 grams per day of L-ornithine-L-aspartate or placebo for two weeks.8 Those taking the ornithine had significant improvements in liver function and blood tests compared to those taking placebo.
Preliminary 9 and controlled 10 studies of people with severe burns showed that supplementation with 10–30 grams of ornithine alpha-ketoglutarate per day significantly improved wound healing and decreased the length of hospital stays.
Where is it found?
As with amino acids in general, ornithine is predominantly found in meat, fish, dairy, and eggs. Western diets typically provide 5 grams per day. The body also produces ornithine.
Ornithine has been used in connection with the following condition (refer to the individual health concern for complete information):
Secondary Burns
Liver cirrhosis (hepatic encephalopathy)
Recovery from illness
Athletic performance (for body composition and strength)
Who is likely to be deficient?
Since ornithine is produced by the body, a deficiency of this nonessential amino acid is unlikely, though depletion can occur during growth or pregnancy, and after severe trauma or malnutrition.11
How much is usually taken?
Most people would not benefit from ornithine supplementation. In human research involving ornithine, 5–10 grams are typically used per day, sometimes combined with arginine.
Are there any side effects or interactions?
No side effects have been reported with the use of ornithine, except for gastrointestinal distress with intakes over 10 grams per day.
The presence of arginine is needed to produce ornithine in the body, so higher levels of this amino acid should increase ornithine production.
At the time of writing, there were no well-known drug interactions with ornithine.
References:
1. Bucci LR, Hickson JF, Wolinsky I, et al. Ornithine supplementation and insulin release in bodybuilders. Int J Sport Nutr 1992;2:287–91.
2. Fogelholm GM, Naveri HK, Kiilavuori KT, et al. Low-dose amino acid supplementation: no effects on serum human growth hormone and insulin in male weightlifters. Int J Sport Nutr 1993;3:290–7.
3. Lambert MI, Hefer JA, Millar RP, et al. Failure of commercial oral amino acid supplements to increase serum growth hormone concentrations in male body-builders. Int J Sport Nutr 1993;3:298–305.
4. Bucci L, Hickson JF et al. Ornithine ingestion and growth hormone release in bodybuilders. Nutr Res 1990;10:239–45.
5. Elam RP, Hardin DH, Sutton RA, et al. Effects of arginine and ornithine on strength, lean body mass and urinary hydroxyproline in adult males. J Sports Med Phys Fitness 1989;29:52–6.
6. Cynober L. place des nouveaux substrats azotés en nutrition artificielle périopératoire de l’adulte. Nutr Clin Métabole 1995;9:113 [in French].
7. Brocker P, Vellas B, Albarede JL, Poynard T. A two-centre, randomized, double-blind trial of ornithine oxoglutarate in 194 elderly, ambulatory, convalescent subjects. Age Ageing 1994;23:303–6.
8. Stauch S, Kircheis G, Adler G, et al. Oral L-ornithine-L-aspartate therapy of chronic hepatic encephalopathy: results of a placebo-controlled double-blind study. J Hepatol 1998;28:856–64.
9. Cynober L. Amino acid metabolism in thermal burns. JPEN 1989;13:196.
10. De Bandt JP, Coudray-Lucas C, Lioret N, et al. A randomized controlled trial of the influence of the mode of enteral ornithine alpha-ketoglutarate administration in burn patients. J Nutr 1998;128:563–9.
11. Zieve L. Conditional deficiencies of ornithine or arginine. J Am Coll Nutr 1986;5:167–76. [review]
Kisses unleash chemicals that ease stress levels Rodin's KISS
Chemicals in the saliva may be a way to assess a mate, Wendy Hill, dean of the faculty and a professor of neuroscience at Lafayette College, told a meeting of the American Association for the Advancement of Science on Friday.
In an experiment, Hill explained, pairs of heterosexual college students who kissed for 15 minutes while listening to music experienced significant changes in their levels of the chemicals oxytocin, which affects pair bonding, and cortisol, which is associated with stress. Their blood and saliva levels of the chemicals were compared before and after the kiss.
Both men and women had a decline in cortisol after smooching, an indication their stress levels declined.
For men, oxytocin levels increased, indicating more interest in bonding, while oxytocin levels went down in women. "This was a surprise," Hill said.
In a test group that merely held hands, chemical changes were similar, but much less pronounced, she said.
The experiment was conducted in a student health center, Hill noted. She plans a repeat "in a more romantic setting."
Hill spoke at the session on the Science of Kissing, along with Helen Fisher of Rutgers University and Donald Lateiner of Ohio Wesleyan University.
Fisher noted that more than 90 percent of human societies practice kissing, which she believes has three components — the sex drive, romantic love and attachment.
The sex drive pushes individuals to assess a variety of partners, then romantic love causes them to focus on an individual, she said. Attachment then allows them to tolerate this person long enough to raise a child.
Men tend to think of kissing as a prelude to copulation, Fisher said. She noted that men prefer "sloppy" kisses, in which chemicals including testosterone can be passed on to the women in saliva. Testosterone increases the sex drive in both males and females.
"When you kiss an enormous part of your brain becomes active," she added. Romantic love can last a long time, "if you kiss the right person."
Lateiner, a classical scholar, observed that kissing appears infrequently in Greek and Roman art, but was widely practiced, despite the spread of skin disease at that time by facial kissing. And there was a potential for social faux pas by kissing the wrong person at the wrong time.
Overall, the science of kissing — philematology — is under-researcherd, Hill concluded.
[By RANDOLPH E. SCHMID, AP Science Writer Randolph E. Schmid, Ap Science Writer – Fri Feb 13, 6:22 pm ET]
Eurojust supports wire-tapping of Skype conversations, skype conversations recorded
EUOBSERVER / BRUSSELS – EU's judicial cooperation agency Eurojust will take the lead in finding ways to help police and prosecutors across Europe to wiretap computer-to-computer phone conversations enabled by programs such as Skype.
"We will sit together with all member states to see how this can be done technically and legally," Joannes Thuy, Eurojust spokesman told this website.
Mr Thuy stressed that the wiretapping would not affect "normal users", but would have to be carried out only as part of a criminal investigation.
Eurojust's talks with prosecutors and police officials from member states, as well as legal experts would be led by Italian prosecutor Carmen Manfreda.
"There are 30 different legal systems all across the EU, so we expect the talks to take several months before first results are presented," Mr Thuy added.
Skype, an Danish-Swedish business developed by Estonian programmers that was sold to E-Bay in 2005 and has over 350 million customers worldwide, is said to be un-spyable by intelligence services.
In its press release, Eurojust says that "Skype has so far refused to share its encryption system with national authorities."
However, Skype claims that it has "extensively debriefed Eurojust on our law enforcement programme and capabilities."
"Skype cooperates with law enforcement where legally and technically possible. Skype remains interested in working with Eurojust despite the fact that they chose not to contact us before issuing this inaccurate report," Brian O'Shaughnessy, head of corporate communications at Skype said in a statement.
The Italian anti-mafia prosecutors requested Eurojust to coordinate this initiative, pointing that criminals in Italy were increasingly making phone calls over the internet in order to avoid getting caught through mobile wiretapping.
Bavarian authorities allegedly also attempted to wiretap Skype conversations and commissioned an IT firm to do this, but were not successful, according to documents obtained by Piraten Party, a movement promoting Internet freedom.
According to Eurojust, customs and tax police in Milan have overheard a suspected cocaine trafficker telling an accomplice to switch to Skype in order to get details of a 2kg drug consignment.