Venezuela has the largest proven oil reserves in the world. It was once so rich that Concorde used to fly from Caracas to Paris. But in the last three years its economy has collapsed. Hunger has gripped the nation for years. Now, it’s killing people and animals that are dying of starvation. The Venezuelan government knows, but won’t admit it!!! Four in five Venezuelans live in poverty. People queue for hours to buy food. Much of the time they go without. People are also dying from a lack of medicines. Inflation is at 82,766% and there are warnings it could exceed one million per cent by the end of this year. Venezuelans are trying to get out. The UN says 2.3 million people have fled the country - 7% of the population.
Showing posts with label Chez Chicas. Show all posts
Showing posts with label Chez Chicas. Show all posts

Friday, October 12, 2012

What if Cannabis Cured Cancer (Serbian subtitle)


What if Cannabis Cured Cancer 

(Serbian subtitle) video

Could the chemicals found in marijuana prevent and even heal several deadly cancers? Could the tumor regulating properties of cannabinoids someday replace the debilitating drugs, chemotherapy, and radiation that harms as often as it heals? Discover the truth about this ancient medicine as world renowned scientists in the field of cannabinoid research explain and illustrate their truly mind-blowing discoveries. QUOTES: "What If Cannabis Cured Cancer summarizes the remarkable research findings of recent years about the cancer-protective effects of novel compounds in marijuana. Most medical doctors are not aware of this information and its implications for prevention and treatment. If we need more evidence that our current policy on cannabis is counterproductive and foolish, here it is." -Andrew Weil, M.D. "A hugely important film" - Julie Holland, M.D. NYU School of Medicine Written by Anonymous

watch here



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Oncologist Donald Abrams defends Medical Cannabis on NPR’s “Science Friday”


Listen to the podcast here:
Feds to Debate Marijuana as Medicine
Transcript from NPR:
The federal government lists marijuana as a Schedule I controlled substance—meaning it has no medically accepted use. Next week, interest group Americans for Safe Access will present the scientific case for marijuana’s therapeutic effects to a federal appeals court, in hopes of relaxing federal restrictions. Oncologist Donald Abrams reviews the evidence on cannabis.

Published: October 12, 2012
IRA FLATOW, HOST:
Next Tuesday, marijuana will have its day in court because the United States Court of Appeals is set to hear arguments about the drug’s therapeutic and medicinal effects. But some doctors, like one of my next guests, disagrees with the government’s ban on medical use of marijuana, pointing to the drug’s ability to suppress nausea, stimulate the appetite, relieve pain, improve sleep, even fight cancer cells, in test tubes at least.
Is the science on cannabis compelling enough to convince federal officials? And have we done the rigorous science on marijuana that’s required of all drugs to get it to your pharmacy? Dr. Donald Abrams is chief of oncology at San Francisco General Hospital. He’s also a professor of medicine at the University of California in San Francisco. He joins us by phone. Welcome to SCIENCE FRIDAY, Dr. Abrams.
DR. DONALD ABRAMS: Thank you, good to be here.
FLATOW: You’re welcome. Dr. Bertha Madras is professor of psychology – psychobiology, I’m sorry, in the Department of Psychiatry at Harvard Med School in Southborough, Massachusetts. She joins us by phone. Welcome to SCIENCE FRIDAY.
DR. BERTHA MADRAS: Thank you, good afternoon.
FLATOW: Good afternoon to you. Dr. Abrams, do you think it’s time? Do you think the evidence is there that the federal government should OK cannabis for general use?
ABRAMS: Well, I mean, let’s take a step back. Cannabis was on the formulary of the United States until 1942, when it was removed. So cannabis, which has been a medicine for thousands of years in other parts of the world, was available in this country, again, until ’42, when it was taken off our pharmacopoeia. So yes, I think that the Institute of Medicine in their last report in 1999 suggested that cannabis and cannabinoids, their active components, have use in treatment of nausea, vomiting, pain and loss of appetite.
And as a cancer doctor, I see patients every day, people who are benefitting from the use of cannabis. The problem is the government does not allow cannabis to be studied as a therapeutic agent because the only legal source is the National Institute on Drug Abuse, and they have a congressional mandate only to study substances abused as substances of abuse. So that’s a bit of a catch-22.
FLATOW: Dr. Madras, would you agree with that?
MADRAS: Frankly I disagree, and here are my reasons why. Number one is, yes, marijuana was removed from the pharmacopeia in the late 1930s, in fact, but because it was found that the safety and efficacy issues did not reach the bar that was necessary for drug approval.
The fact that Dr. Abrams claims that we cannot study cannabis in scientific studies is disingenuous because the Center for Medicinal Cannabis Research, of which he’s a part of, in California, has conducted and has received millions of dollars from the California Legislature to study smoked marijuana as a medicine.
And as of today, I have looked at their site. They have precisely four published manuscripts on the medicinal uses of cannabis for which the Proposition 15 approved marijuana and a number of other publications that bear no relationship to these clinical trials.
So the clinical trials can go on. The marijuana is available for them. Cannabinoids are being studied and synthesized at horrendously large rates by medicinal chemists, and yet…
FLATOW: I have to interrupt you. We’ll get back to you, Dr. Madras. We have to take a break. Stay with us. Also Dr. Abrams, we’ll be right back after this break. I’m Ira Flatow, this is SCIENCE FRIDAY from NPR.
(SOUNDBITE OF MUSIC)
FLATOW: This is SCIENCE FRIDAY. I’m Ira Flatow. We’re talking this hour about legalization of cannabis and the use of cannabis, otherwise marijuana, in research studies. When I interrupted Dr. Bertha Madras, she was talking about the fact that there were lots of studies in California and plenty of samples of cannabis to get if you needed to study it. Dr. Abrams, how do you answer that?
ABRAMS: Yeah, so the Center for Medicinal Cannabis Research was set up in California for that reason, to fund studies to look at the potential effectiveness of cannabis. And I did two, one that demonstrated in patients with HIV and painful nerve damage cannabis was better than placebo in relieving their pain.
And I also did a study funded actually by NIDA because it was a safety study to show that it was safe for patients on chronic opiates to add cannabis to their regimen. It did not change the level of opiates in their bloodstream, and if anything, it may have improved their pain relief.
FLATOW: So you think there’s enough evidence, then, that the courts should approve it?
ABRAMS: Well, no, you know, again, evidence, that’s what I’m saying. It’s difficult to do clinical trials looking at cannabis as a therapy because of the catch-22 that NIDA, you know, is preferentially supplying their cannabis to studies that look at its danger.
So the evidence, you know, clinically the evidence is there, and I do disagree that the reason that it was removed from the pharmacopeia, the American Medical Association in 1937, after the introduction of the Cannabis Tax Act, was – stood alone in saying that there is no evidence that cannabis is dangerous and that this act would impede the ability to research it for its effectiveness.
And then it was removed from the pharmacopeia and subjected to Schedule 1, and, you know, the main target in this country’s failed war on drugs.
FLATOW: So you think there are not enough resources to conduct the clinical studies that would be needed?
ABRAMS: Well, not many people want to study cannabis. It’s sort of a difficult thing in your career because, you know, I think the more – science is not driving the train, that’s what I’ll say. I mean, the more evidence that people accumulate – we now have three studies demonstrating cannabis’ utility in peripheral neuropathy, which is a very challenging medical condition to treat.
Oftentimes people are put on opiates, and then their life is one string of opiates after another. Better – cannabis, this is a flower we’re talking about it. It’s a flower. It’s not a dangerous substance like the opiates that I prescribe and others prescribe for patients living with cancer and pain.
FLATOW: Dr. Madras, would you acknowledge that cannabis and cannabinoids have some therapeutic effects like Dr. Abrams mentioned?
MADRAS: I acknowledge that cannabinoids may have some therapeutic effects. I disagree with Dr. Abrams vehemently on the thought that one’s hands are tied in doing the science. Once again, the Centers for Medicinal Cannabis…
ABRAMS: Oh don’t repeat yourself on that, that’s silly.
MADRAS: Had all money available to do with – and they have…
ABRAMS: Three million dollars a year for three years.
MADRAS: But let me please finish. They had to cancel five studies because they could not recruit enough patients. One of the criteria for recruiting patients is that they had to be experienced marijuana users. How many elderly cancer patients in this day and age are experienced marijuana users? They also are not allowed to drive because there was fear of liability in case they got into a car accident because they were under the influence.
So there – so what Dr. Abrams should say is that there was money, there was cannabis available for the studies. Why did five of the major studies that they had proposed at the onset of this program, why were they canceled?
FLATOW: Dr. Abrams, any answer?
ABRAMS: Well, I mean, you know, again, all of my studies were done in the in-patient clinical research center so we could observe the patients and make sure they weren’t diverting this Schedule 1 substance. And cancer patients, I don’t think, are that enthusiastic about spending, you know, some of the remaining days of their lives in the hospital doing a research study.
Plus there was always a concern that the cannabis that NIDA provides is not particularly potent and that because we live in California, where we’ve had cannabis available as a medicine for patients since 1996, if patients really wanted to use it, they could.
And as a cancer doctor, ma’am, many patients in my age group, who grew up in the ’60s and ’70s, with cancer are cannabis-experienced people. So that is not a problem. The problem is the closing of the dispensaries now by the federal government in California, when we voted for it in 1996, is not allowing my elderly patients access to their medicine.
MADRAS: And NIDA provides marijuana cigarettes at 3.5 and seven percent THC. Do you think that you need more than that, especially considering one of the studies that came out of the CMCR that said that at seven percent the side effects were quite above the boundary of acceptable side effects, meaning psychoactive dizziness, confusion and so on?
So my feeling is that the doses that are available for this research are in fact available, but once you get into seven percent or six percent cannabis, you do have side effects that have to be reported in clinical trials, far beyond that boundary of what are…
ABRAMS: Yeah. Again, I hate to disagree with you, but the cannabis available in dispensaries averages from 10 to 15 percent, and legal cannabis in The Netherlands is 14 percent that you get from the pharmacy. So three and seven percent is not a huge amount, and I think patients need to self-titrate.
It’s very different from other medicines, you know, where you tell the patient try it and see what works for you. You know, if it…
MADRAS: But that’s not how the FDA works.
ABRAMS: Well, of course not. This is not…
MADRAS: The FDA requires and insists that one does a window of therapeutic efficacy compared with a window of a side effect profile that may render a drug unacceptable in the market. And if you do a full-dose response curve, you will find that past a certain percentage of THC, a person is quite incompetent.
ABRAMS: Well, that’s absolutely correct, same with alcohol. You know, I mean, I personally believe that this is a flower, and it should be regulated like tobacco or alcohol. And, you know, trying to get FDA approval for a medicine that’s been a medicine for thousands of years and was on the U.S. pharmacopeia until 1942, when it was removed by an act of Congress submitted by a racist, you know, what are we doing in this country.
This is a flower. We’re spending $4 billion a year on the war on drugs and incarcerating 180,000 Americans.
MADRAS: Well, you know, ephedrine from the ma huang plant…
ABRAMS: Oh, you could give me all the examples you want. I’m not in favor of cocaine, either.
MADRAS: Pardon? Most of our medications, at least 30 percent, are originally derived from plants.
ABRAMS: Right.
MADRAS: The active ingredients were isolated, such as cocaine, such as digitalis, such as aspirin, such as morphine. They were isolated. They were studied in isolation in order to determine how fast they get into the brain, how fast they get into the blood…
ABRAMS: That’s the Western pharmaceutically dominated paradigm, you know…
MADRAS: And also what the…
FLATOW: I’m going to jump in here. I’m going to jump in, and I’m going to ask…
ABRAMS: There are thousands of years of research where people use the whole plant as medicine.
FLATOW: Dr. Abrams, do you think it’s possible to create studies that would satisfy the FDA requirements?
ABRAMS: I’m sorry, I do not. I continue to do this work, but I don’t think that this is going to happen in my lifetime unless other people start looking at the ridiculousness of our current policies in this country. I’m sorry.
FLATOW: Ridiculous meaning what?
ABRAMS: Well, this is a flower. You know, I grew up in the ’60s and ’70s. I went to Brown University and Stanford University School of Medicine. Cannabis was my substance of choice, not alcohol. And I’m very happy with the person that I’ve become today, and I would be very different if alcohol was what I used for relaxation.
FLATOW: Dr. Madras, have you done studies on cannabis?
MADRAS: I have done a few limited studies on isolated cannabinoids, not in patients, in preclinical research. I have studied the literature extensively because I am very interested in the scientific issues, not as much the political issues.
FLATOW: Well, do you believe that the studies…
ABRAMS: Science does not drive the politics…
MADRAS: I believe…
FLATOW: Dr. Madras, do you believe that studies can be done that would satisfy the FDA?
MADRAS: I certainly do.
ABRAMS: Oh, my goodness.
MADRAS: I think that…
FLATOW: And who would do them?
MADRAS: Well, (unintelligible)…
ABRAMS: Good question.
MADRAS: …and I have no, you know, full disclosure, I have absolutely no outside funding from any sources.
FLATOW: So who should do this? Who should get the funding to do this?
MADRAS: So drug companies – RGW Pharmaceuticals in England, they’ve approved an inhaled form of…
ABRAMS: It’s not inhaled, dear. It’s sprayed under the tongue.
MADRAS: …THC combined with cannabidiol, which does not have psychoactive effects but therapeutic effects and different types of formularies that can deliver a reasonable bolus of active…
FLATOW: Well, Great Britain…
MADRAS: …ingredients to the brain would satisfy the FDA. At this point, the real issue is the relationship between psychoactive effects and therapeutic effects. The faster a drug gets into the brain, the more addictive it – more…
ABRAMS: No. Don’t start with addictive.
MADRAS: …addictive potential and the more its psychoactive effects. And this is the problem with a substance such as marijuana smoke. The other issue is: Do we want smoked marijuana as a delivery system for medications? It has between 60 and 80 cannabinoids in it of uneven quantities because every one produces different ratios…
FLATOW: OK.
MADRAS: …of all of them.
FLATOW: I have to stop you from filibustering. Let me get another question in here. Dr. Abrams, for people who already have problems, health problems, what about the smoking issue? Isn’t smoking a bad solution?
ABRAMS: Yeah. My friend and colleague Donald Tashkin at the University of California, Los Angeles has spent 40 years of his career doing studies for NIDA looking for the danger of inhaling cannabis and basically finds that chronic users may have a little bronchitis. Actually, it appears from his (unintelligible) study of 1,365 patients with aerodigestive malignancies in Los Angeles that regular cannabis use decreased the risk of lung cancer. A recent study in young people followed for 20 years show that those who regularly use cannabis had better pulmonary function tests than those who didn’t.
So there are other ways to deliver cannabis than smoking, and we’ve investigated a vaporizer, and vaporization is now widely used by patients here in California as a smokeless delivery system. But in my opinion, smoking is not that dangerous, either, and I’m sure that will get some disagreement from my colleague.
FLATOW: A lot of people think that it’s the high that you get from smoking marijuana that is the therapeutic effect. Is that correct?
ABRAMS: I think that the cannabinoids – we have two receptors in our bodies, the CB1, which is in the brain, and the CB2, which is in the immune system. And the activation of these receptors causes chemical reactions in cells which have many different effects besides the psychoactivity. As my colleague said, another cannabinoid, cannabidiol is very potently analgesic and anti-inflammatory without being psychoactive. So the concern that there’s 60 or 70 other cannabinoids in the plant is exactly something, I think, is a good thing.
As a student of traditional Chinese medicine, a medicine that’s been practiced for 5,000 years, they frequently use the whole plant instead of following the Western pharmaceutically industry dominated paradigm of isolating the active component, make it into a pill that people swallow and charging large amounts of money. So I think that the cannabinoids, as well as the other components of the plant – terpenoids and flavonoids – all have the potential for medical benefits.
FLATOW: All right. Let me remind everybody that this is SCIENCE FRIDAY from NPR. Let me ask you, Dr. Madras, one more time, do you think there are studies that can be done in the United States that would convince the FDA, and who would do them?
MADRAS: I think there are studies. I think we have to, A, alter the delivery system to remove smoke. Marijuana smoke has ammonia up to 20 times greater than tobacco smoke. It has hydrogen cyanide and nitric oxide and some aromatic amines that are three to five times higher in marijuana than tobacco smoke. And there are many other problems associated with marijuana smoke. So what are the criteria? One should change the method of delivery…
FLATOW: Who will do…
MADRAS: …and (unintelligible)…
FLATOW: Who will do the study? Ma’am. Ma’am, who will do the study?
MADRAS: …(unintelligible) change the method of delivery as well as study and…
FLATOW: Dr. Madras, who will…
MADRAS: …focus on single cannabinoids.
FLATOW: Dr. Madras, who will do these studies?
MADRAS: Well, there are pharmaceutical companies that are quite interested in…
FLATOW: Have they – will they…
ABRAMS: It’s a flower. Nobody can patent a flower.
FLATOW: Will they…
ABRAMS: Nobody can patent a flower. They’re not going to make any money.
FLATOW: Who’s going to…
MADRAS: They can patent methods of delivery. They can patent single isolated cannabinoids. They can (unintelligible)…
ABRAMS: And they’ve done that. We have that on the market.
MADRAS: They can (unintelligible).
ABRAMS: That’s called dronabinol and nabilone. Those are available for patients. I’ll tell you, as a cancer doctor, I’m…
MADRAS: Yes. Generic drugs are very, very lucrative for companies such as Teva Pharmaceuticals. They can be made as generics as well.
FLATOW: Who will? Can is a large population. Who is doing it and will do it and pay for it?
ABRAMS: Can I – there’s no answer to that, so I can just say as a cancer doctor now for 30 years in a state where we have tolerance to the use of cannabis as medicine, that a day doesn’t go by when I don’t see a cancer patient who has nausea, loss of appetite, pain, depression and insomnia. And I could recommend one medicine to that patient and instead of writing prescriptions for five or six different pharmaceuticals that may interact with each other or with the patient’s chemotherapy. And this is a medicine that my cancer patients can grow if they want to.
I ask all of my patients: What brings you joy? And the percentage of people living and, in fact, dying with cancer who tell me gardening brings them joy is not insubstantial because bringing life out of the ground is a pleasure. And if this life that people bring out of the ground is also their medicine, why don’t we let them have it? The number of patients who come to me saying they were given narcotics and at their – the end of life and they can’t communicate with their family, and then they wean themselves off of their opiates with cannabis so that they could have a more pleasurable interaction in their final days of life. Why do we deny people this medicine?
MADRAS: Well, why is it that the recommendations currently are that serotonin 5-HT3 antagonists are much better at preventing chemotherapy-induced nausea than marijuana?
ABRAMS: Yeah, I’m not going to – it’s not a question about ranking, but I think…
MADRAS: Why is that there are so many alternatives now to smoking marijuana, sending the wrong message to kids…
ABRAMS: I hope you never have to repeat chemotherapy.
MADRAS: …than what you’re claiming? I’m afraid…
ABRAMS: Right. But what about Melissa Etheridge? She’s the one that went public, saying she could not have tolerated her chemotherapy for her breast cancer if she didn’t use cannabis. We have many medicines, but if they don’t work and cannabis does, why deprive people of their medicine?
FLATOW: All right. I have to stop it right there. Dr. Bertha Madras, professor of psychobiology at the Department of Psychiatry at Harvard. Dr. Donald Abrams, chief of oncology, San Francisco General Hospital. Thank you both for taking time to be with us.
ABRAMS: Sure.
Dr Madras, there are MANY other delivery systems for medical cannabis, check us out!http://www.cannakitchenandresearch.com/menu-of-products.html


THANK YOU http://patients4medicalmarijuana.wordpress.com !!!

More info: http://patients4medicalmarijuana.wordpress.com/2012/10/12/oncologist-donald-abrams-defends-medical-cannabis-on-nprs-science-friday/
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Thank you for your time,
Hope you'll found the information you expected,
Don't hesitate contacting us,
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Appeals Court to Consider Benefits of Medical Marijuana


Appeals Court to Consider Benefits of Medical Marijuana


Associated Press
For the first time in 20 years, a federal court will review scientific evidence on the therapeutic value of marijuana, as a legal challenge by a group of doctors, medical professionals and patients makes its way to the U.S. court of appeals in Washington, D.C., next week.
Americans for Safe Access is hoping the challenge will change the government’s classification of marijuana from a dangerous drug with no medical benefits, the Guardian reported. Other groups, such as the American Medical Association, the American College of Physicians, the American Nurses Association, the Federation of American Scientists and the American Academy of Family Physicians support either medical access to marijuana or its reclassification to one that has a medical benefit.
“Medical marijuana patients are finally getting their day in court,” Joe Elford, chief counsel for ASA, told the Guardian. “This is a rare opportunity for patients to confront politically motivated decision-making with scientific evidence of marijuana’s medical efficacy.”
Last year, the Drug Enforcement Agency rejected the ASA’s petition to reschedule marijuana, saying there wasn’t substantial evidence the drug should be removed from schedule 1. The DEA cited a five-year-old assessment from the Department of Health and Human Services that said there was no consensus in the medical community on the medical applications of marijuana.
In its reply brief, the ASA says the criteria used by the DEA and HHS to determine scheduling are flawed.
The U.S. Court of Appeals for the D.C. Circuit will hear arguments in the case on Oct. 16.


More info: http://blogs.wsj.com/law/2012/10/08/appeals-court-to-consider-theraputic-value-of-medical-marijuana/
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Marijuana Cuts Growth of Lung Cancer Tumor in Half


Marijuana Cuts Growth of Lung Cancer Tumor in Half


Delta-tetrahydrocannabinol (THC), the active ingredient in marijuana, has the potential to cut tumor growth in common lung cancer in half and significantly reduce the ability of the cancer to spread. This finding was disclosed by researchers at Harvard University who tested the chemical in both lab and mouse studies.
The compound inhibits EGF-induced growth and migration in epidermal growth factor receptor (EGFR) expressing non-small cell lung cancer cell lines. It is worthwhile to note that lung cancers, which are characterized by over-expression of EGFR, are generally highly aggressive and resistant to chemotherapy.
The active marijuana ingredient is similar in function to endocannabinoids and targets cannabinoid receptors CB1 and CB2. Endocannabinoids are naturally-producing cannabinoids in the body and activate the receptors CB1 and CB2.
It was suggested by the researchers that Delta-tetrahydrocannabinol (THC) or other designer agents that activate these receptors could be used in a targeted manner for treating lung cancer.
“The beauty of this study is that we are showing that a substance of abuse, if used prudently, may offer a new road to therapy against lung cancer,” said Anju Preet, Ph.D., a researcher in the Division of Experimental Medicine.
Endocannabinoids (as well as THC), acting through cannabinoid receptors CB1 and CB2, are considered to play a role in variety of biological functions, such as pain control and inflammation. Even though Marinol, a medical derivative of THC, is approved for use as an appetite stimulant for cancer patients, and a small number of U.S. states allow use of medical marijuana for treating the same side effects, few studies have suggested that THC could have anti-tumor activity, according to Preet.
Researchers, in the present study, demonstrated that two different lung cancer cell lines and patient lung tumor samples express CB1 and CB2. It was also suggested that non-toxic doses of THC inhibited growth and spread in the cell lines. “When the cells are pretreated with THC, they have less EGFR stimulated invasion as measured by various in-vitro assays,” Preet said.
During the study, the researchers injected standard doses of THC into mice that had been implanted with human lung cancer cells for three weeks. They found that tumors were reduced in size and weight by about 50 percent in treated animals compared to a control group. The researchers were also able to notice a 60 percent reduction in cancer lesions on the lungs in these mice as well as a significant reduction in protein markers associated with cancer progression, Preet says.
The researchers said the substance could be activating molecules that arrest the cell cycle though they were clueless as to why THC inhibits tumor growth. It was speculated that THC may also interfere with angiogenesis and vascularization that promotes growth of cancer.
“THC offers some promise, but we have a long way to go before we know what its potential is,” Preet said. Preet also suggested that there is much work required for clarifying the pathway by which THC functions, and cautions that some animal studies have shown that THC could stimulate some cancers.

References:
American Association for Cancer Research http://www.aacr.org/

thank you imarijuana.com !!!


More info: http://www.imarijuana.com/medical-marijuana/marijuana-cuts-growth-of-lung-cancer-tumor-in-half
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Larry King Talks Marijuana Legalization: 'I Think It Will Be Legal' (VIDEO)


Larry King spoke about the legalization of marijuana Wednesday on HuffPost Live.
King said he has "always felt" that marijuana should be legal, arguing that it was legally available until the liquor industry intervened, and claiming that it helps sick people.
"I know that it helps ill people," he told HuffPost Live's Jacob Soboroff and Alyona Minkovski. "I know it's great used with cataracts. I think it will be legal."
King said he thinks that legalization would be "logical" and that marijuana is OK "in moderation."
"I don't think you should smoke marijuana and drive," he cautioned.

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Thank you for your time,
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Russia suspends import and use of American GM corn after study revealed cancer risk Read more: http://www.dailymail.co.uk/news/article-2208452/Russia-suspends-import-use-American-GM-corn-study-revealed-cancer-risk.html#ixzz2983xl4bp Follow us: @MailOnline on Twitter | DailyMail on Facebook


Russia suspends import and use of American GM corn after study revealed cancer risk  



  • The European Food Safety Authority orders review in to the research, conducted at a French university
  • Russia's decision could be followed by other nations
  • Experts at the University of Caen conducted an experiment running for the full lives of rats - two years
  • The findings found raised levels of breast cancer, liver and kidney damage
  • The same trials also found minuscule amounts of a commonly used weedkiller, Roundup
  • Both the GM corn and Roundup are the creation of US biotech company Monsanto


  • Russia has suspended the import and use of an American GM corn following a study suggesting a link to breast cancer and organ damage.
    Separately, the European Food Safety Authority(EFSA), has ordered its own review in to the research, which was conducted at a French university.
    The decision by Russia could be followed by other nations in what would be a severe blow to the take-up of the controversial technology.
    Cancer risk? A farmer shows two corncobs of genetically engineered corn by U.S. company Monsanto, right, and two normal corncobs from Germany, left
    Cancer risk? A farmer shows two corncobs of genetically engineered corn by U.S. company Monsanto, right, and two normal corncobs from Germany, left
    Historically, biotech companies have proved the safety of GM crops based on trials involving feeding rats for a period of 90 days.
    However, experts at the University of Caen conducted an experiment running for the full lives of rats - two years.
    The findings, which were peer reviewed by independent experts before being published in a respected scientific journal, found raised levels of breast cancer, liver and kidney damage.

    The same trials also found evidence that consumption of minuscule amounts of a commonly used weedkiller, Roundup, was associated with a raised risk of cancer.
    Both the GM corn, which carries the name NK603, and Roundup are the creation of US biotech company Monsanto.
    The decision by the Russians to suspend authorisation for the American GM corn threatens to trigger a transatlantic commercial and diplomatic row.
    Contentious: A combine harvests corn in a field near Coy, Arkansas. The decision by the Russians to suspend authorisation for the American GM corn threatens to trigger a transatlantic commercial and diplomatic row
    Contentious: A combine harvests corn in a field near Coy, Arkansas. The decision by the Russians to suspend authorisation for the American GM corn threatens to trigger a transatlantic commercial and diplomatic row
    Russia’s consumer rights watchdog, Rospotrebnadzor, said today that it has suspended the import and use of the Monsanto GM corn.
    Rospotrebnadzor said the country’s Institute of Nutrition has been asked to assess the validity of the study. 
    It has also contacted the European Commission’s Directorate General for Health & Consumers to ask for the EU’s position on the corn’s safety.
    Consumer scepticism in the UK and Europe means GM corn is not on supermarket shelves here, however it is fed to farm animals, including hens, pigs and dairy cows.
    Important: In the USA, and much of Europe, corn is used to make an array of food products including cornflakes (picture posed by model)
    Important: In the USA, and much of Europe, corn is used to make an array of food products including cornflakes (picture posed by model)
    Last week Monsanto said it did not think the French study would affect its license to export the NK603 to Europe but would wait to hear from EFSA.
    The company said: ‘Based on our initial review, we do not believe the study presents information that would justify any change in EFSA’s views on the safety of genetically modified corn products or alter their approval status for genetically modified imports.’ 
    The biotech industry and university researchers involved in GM research have mounted a major PR campaign over the last year to win over sceptical consumers.
    In the past week, pro-GM scientists have been lining up to undermine the French experiments and criticise the way they were conducted.
    However, a number of independent academics have praised the French team’s work, describing it as the most thorough and extensive feeding trials involving GM to date.
    Mustafa Djamgoz, the Professor of Cancer Biology, at Imperial College, London, said the findings relating to eating GM corn were a ‘surprise’.
    Prof Djamgoz, who describes himself as a neutral on GM, said: ‘The results are significant. The experiments are, more or less, the best of their kind to date.’ 
    However, he said that it is now important to ensure they are repeated with more animals by independent laboratories to confirm the outcome.
    ‘We are not scaremongering here. More research, including a repetition of this particular study are warranted,’ he said.
    The professor said it will take two to three years to get a definitive answer.

  • More info:http://www.dailymail.co.uk/news/article-2208452/Russia-suspends-import-use-American-GM-corn-study-revealed-cancer-risk.html#ixzz2983xl4bp 
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