The Truth About Cancer Featuring: Jeffrey Smith Talks About the Monsanto Lawyer Turned FDA "Food Safety Czar"

In this video, cancer researcher Ty Bollinger speaks with Jeffrey M. Smith, a leading expert how it can be that companies are allowed to spray Roundup on our food without warning the consumer about the potential dangers. The full interview with Jeffrey is part of "A Global Quest" docu-series.

Support our mission by commenting and sharing with your friends and family below.

About The Truth About Cancer:
 The Truth About Cancer’s mission is to inform, educate, and eradicate the pandemic of cancer in our modern world. Every single day, tens of thousands of people just like you are curing cancer (and/or preventing it) from destroying their bodies. It’s time to take matters into your own hands and educate yourself on real cancer prevention and treatments. It could save your life or the life of someone you love.

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About Ty Bollinger
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Ty Bollinger is a devoted husband, father, a best-selling author, and a Christian. He is also a licensed CPA, health freedom advocate, cancer researcher, former competitive bodybuilder, and author of the best-selling book "Cancer - Step Outside the Box," which has sold over 100,000 copies worldwide.

After losing his mother and father and several family members to cancer, Ty’s heartbreak and grief coupled with his firm belief that chemotherapy, radiation, and surgery were the NOT the most effective treatments available for cancer patients led him on a path of discovery.

He began a quest to learn everything he possibly could about alternative cancer treatments and the medical industry. What he uncovered was shocking. On his journey, he’s interviewed cutting-edge scientists, leading alternative doctors, and groundbreaking researchers to learn about hidden alternative cancer treatments. What he uncovered help to create The Truth About Cancer and its 3 awe-inspiring docu-series’:”The Quest for The Cures”, “The Quest For The Cures Continues”, and “The Truth About Cancer: A Global Quest.”

Ty has touched the hearts and changed the lives of thousands of people around the world. Ty speaks frequently at conferences, local health group meetings, churches, and is a regular guest on multiple radio and TV shows and writes for numerous magazines and websites.

The Truth About Cancer- Jeffrey Smith Talks About the Monsanto Lawyer Turned FDA "Food Safety Czar"

In this video, cancer researcher Ty Bollinger speaks with Jeffrey M. Smith, a leading expert how it can be that companies are allowed to spray Roundup on our food without warning the consumer about the potential dangers. The full interview with Jeffrey is part of "A Global Quest" docu-series. Find the video transcript here: http://bit.ly/jeffrey-smith-monsanto-... To watch Episode 1&2 of "A Global Quest" docu-series for FREE, click here: http://bit.ly/a-global-quest-free-yt Visit our website: www.thetruthaboutcancer.com Join TTAC's 900K+ FB fans: http://bit.ly/TTAC-Facebook-YT Follow us on PINTEREST: http://bit.ly/TTAC-Pinterest-YT Find us on INSTAGRAM: http://bit.ly/TTAC-Instagram-YT Support our mission by commenting and sharing with your friends and family below.
-------------------------------------------------- About The Truth About Cancer -------------------------------------------------- The Truth About Cancer’s mission is to inform, educate, and eradicate the pandemic of cancer in our modern world. Every single day, tens of thousands of people just like you are curing cancer (and/or preventing it) from destroying their bodies. It’s time to take matters into your own hands and educate yourself on real cancer prevention and treatments. It could save your life or the life of someone you love. ---------------------------------------------------------------------- Inside The Truth About Cancer Docu-Series --------------------------------------------------------------------- Doctors, researchers, experts, and survivors show you exactly how to prevent and treat cancer in our 3 original docu-series: "The Quest For The Cures”, “The Quest For The Cures Continues”, “The Truth About Cancer: A Global Quest”, and on our website: http://www.thetruthaboutcancer.com In our docu-series you’ll travel with Ty Bollinger who lost both his mother and father to cancer (as well as 5 other family members). Ty travels the country and the globe and sits down with the foremost doctors, researchers, experts, and cancer conquerers to find out their proven methods for preventing and treating cancer. You can watch Episode 1 & 2 NOW for FREE by following this link: http://bit.ly/a-global-quest-free-yt Please join our email list to be notified of all upcoming events (including free airings of our docu-series): http://bit.ly/join-ttac-mission-yt Learn more about our latest docu-series “The Truth About Cancer: A Global Quest” here: http://bit.ly/agq-silver-ttac-yt --------------------------------------- About Ty Bollinger --------------------------------------- Ty Bollinger is a devoted husband, father, a best-selling author, and a Christian. He is also a licensed CPA, health freedom advocate, cancer researcher, former competitive bodybuilder, and author of the best-selling book "Cancer - Step Outside the Box," which has sold over 100,000 copies worldwide. After losing his mother and father and several family members to cancer, Ty’s heartbreak and grief coupled with his firm belief that chemotherapy, radiation, and surgery were the NOT the most effective treatments available for cancer patients led him on a path of discovery. He began a quest to learn everything he possibly could about alternative cancer treatments and the medical industry. What he uncovered was shocking. On his journey, he’s interviewed cutting-edge scientists, leading alternative doctors, and groundbreaking researchers to learn about hidden alternative cancer treatments. What he uncovered help to create The Truth About Cancer and its 3 awe-inspiring docu-series’:”The Quest for The Cures”, “The Quest For The Cures Continues”, and “The Truth About Cancer: A Global Quest.” Ty has touched the hearts and changed the lives of thousands of people around the world. Ty speaks frequently at conferences, local health group meetings, churches, and is a regular guest on multiple radio and TV shows and writes for numerous magazines and websites. ----------------------------------- jeffrey m smith, jeffrey smith gmo, Ty Bollinger, The Truth About Cancer, A Global Quest, Michael Taylor, Monsanto, FDA, gmo foods, effects of gmo foods, gmo food health effects, genetically modified food, gmos, genetically modified organisms, genetically modified crops, monsanto gmo, gmo food, genetically modified foods, what is a gmo, gmo pros and cons, RoundUp, gmo facts, genetic modified food, genetically engineered food, genetically modified corn, gmos in food, gmo health risks, gmo research, genetic modified organisms, gmo in food, how to avoid gmo foods, facts about gmos, what is gmo food, what is genetically modified food, what are gmo foods, genetic engineering food, are gmo foods safe, gmo safety, history of gmos, disadvantages of gmos

Cancer cure was found 100 years ago -- buried by the FDA

The Remarkable Cancer Therapy of a
'Modern Pasteur'

"…the history of the Koch Treatment is more dramatic than anything which the mind of a Hollywood fiction writer could imagine."

So wrote three doctors in Birth of a Science (1957), the story of William F. Koch, MD, PhD., a Detroit man who lived from 1885 to 1967. Dr. Koch is said to have created one of the most remarkable medical therapies of the last century -- a treatment not only for cancer but also for many other diseases. Yet these days it’s a therapy mostly confined to the pages of history.

This is how the story unfolded…and failed to unfold, too.

Continued.... 

FDA Seeks to Outlaw All the New Supplement Discoveries of the Last 17 Years

Back in the early 1990s, the FDA tried to make many supplements illegal. Consumers were so alarmed by the FDA's bullying that they staged a massive revolt. The result was that Congress passed the Dietary Supplement Health and Education Act (DSHEA). That law protected supplements from the FDA unless the FDA could prove a supplement wasn't safe.



There was, however, a loophole in the 1994 law. The FDA was given the authority to regulate new ingredients introduced after October 15, 1994.



So what happened? Nothing at first. For 17 years, the FDA took no action, gave no guidance, and launched no enforcement of these "New Dietary Ingredients."



And that's been a good thing. Because for 17 years, the dietary supplement industry has enjoyed tremendous innovation. These innovations have allowed us to extract and concentrate the most effective natural ingredients. As a result, millions of consumers have benefitted. They've protected their hearts and arteries ... found relief from their joint pain ... boosted their memory ... and more.



And during this time, supplements have enjoyed a remarkable safety record. Statistics show that supplements are safer than prescription drugs, cosmetics, medical devices, and even food!



According to the Poison Control Centers, there were zero deaths due to supplements in 2008. In 2009, there was one.



Supplements the FDA Wants to Ban


But now the FDA wants to act like the last 17 years never happened. The agency has drafted a proposal to regulate what it calls New Dietary Ingredients. If this proposal is implemented, some of the most effective nutrients you take will be pulled from the market. Nutrients like resveratrol ... ubiquinol CoQ10 ... bacopa ... strontium ... and more.



But that's not all. Under these guidelines, the FDA can define almost anything as a "new" dietary ingredient. For example:



* If a supplement includes more of an ingredient than was used 17 years ago — even something like vitamin C — it's "new."

* If an ingredient uses a different extraction process — like baking or fermentation — it's "new."

* If a supplement uses an ingredient at a different "life stage" — such as using ripe rather than non-ripe apples — it's "new."

* If a supplement duplicates an ingredient in a laboratory rather than extracting it from the food — even though it's chemically identical — it's "new."

* And if a probiotic formula includes a strain of bacteria that wasn't found in yogurt 17 years ago, it's "new."




So what would happen to all these "new" ingredients? The manufacturers would have to take them off the market until they could prove the ingredients are safe — even if those ingredients have been safely used for 17 years!



Why It's Nearly Impossible to Comply


What kind of proof is the FDA demanding? According to the guidelines, many companies would have to conduct animal studies using a dosage that's 1,000 times the typical dose.



I'm not kidding you. It's right there in black and white on the FDA's website. The FDA wants vitamin makers to do studies for a full year, at 1,000 times the typical dose.



So a fish-oil manufacturer would have to conduct a one-year study where animals are force-fed the human equivalent of 240,000 milligrams of fish oil each and every day! This outlandish dose would injure the animals and give the FDA an excuse to outlaw the product.



But wait, it gets even better. If one fish-oil manufacturer performs such a study and it passes, it doesn't mean the other fish-oil makers can use the same data. No sir. They are still required to go out and do their own studies before they're allowed to sell their product.



And these studies are very expensive. A study like the one above typically costs about $100,000-$200,000 to perform. Multiply that by several ingredients in several products, and you get an idea of the cost.



Say a company carries 6 products containing 6 ingredients each. It would cost between $3.6 and $7.2 million in studies before that company could even offer the products for sale. For a larger company offering 50 products or more, the costs would be astronomical.



Few supplement makers will be able to afford these studies, and many will be put out of business. And the ones that remain would still be at the mercy of the FDA's whim. That's because there are no requirements for the FDA to approve anything. They can approve or reject anything they want. And in the past, they have rejected the majority of ingredients submitted to them.



That means most of the nutrients you buy today will be pulled from the market and never return. Those that do return will be a lot more expensive — or may only be available as prescription drugs!



A Blatant Abuse of Power


This is a blatant abuse of power. What the FDA is doing here is performing an end-run around the existing law. According to the law, the FDA has to prove a dietary supplement is unsafe for it to be taken off the market. These new guidelines turn that on its head. They are clearly not what Congress intended.



Fortunately, these FDA guidelines have not yet been finalized. All federal agencies are required to give the public an opportunity to comment on a draft before it is made final. In this case, the FDA has given interested parties until December 1st to comment on the draft. That means there's a small window of opportunity for you to voice your disapproval.



Frankly, I wouldn't bother commenting to the FDA. The process is cumbersome, and those unelected bureaucrats don't care what you think anyway.



What You Can Do


The best way to defeat these new rules is to talk to the people you do elect — your congressman and your two U.S. senators. They have the power to rein in the FDA — and they have done so in the past when enough voters complained.



Back in the 1970s, the FDA tried to require "warning labels" on vitamins. Angry voters called and wrote letters, and Congress responded with the Proxmire Amendments which limited the FDA's power.



Then in the 1990s, the FDA went on the warpath again. When voters complained, Congress passed the Dietary Health Supplement Education Act, which once again limited the FDA's power.




But like a monster killed in a horror movie, the FDA keeps coming back. And so once again, it's time for us to step up and call the folks who rely on our votes.



Here's what you need to do:


Go to http://www.usa.gov/Contact/Elected.shtml and look up the phone numbers of your U.S. Senators and your Representative (congressman). Then give them a call.



Don't be shy and don't worry. No one is going to bite you, no one is going to argue with you, and no one is going to quiz you to see how well you know the issues. The job of the staffers who answer is to listen politely and to relay what you say to their boss. So please do call. And please be polite and respectful of the staffers' time.



Here are some talking points to use when you call:


* Hello, my name is [name] and I am a constituent of [name of Senator or Representative].

* I am very concerned about the new FDA draft guidance on dietary supplements and new dietary ingredients.

* [Feel free to tell them about the supplements you take and/or the benefits you get from those supplements. Then feel free to make as many of the following points as you like:]

1. Supplements have an unrivaled safety record. Statistics show they're safer than drugs, safer than medical devices, safer than cosmetics, and even safer than food.

2. The FDA cannot define New Dietary Ingredients so broadly. According to these guidelines, almost everything is a New Dietary Ingredient. This will strangle innovation and deprive consumers of the supplements they depend on for their health.

3. The FDA did nothing about new dietary ingredients for 17 years. Now they want to wipe out 17 years' worth of innovation and 17 years' worth of benefits to the consumer.

4. When the Dietary Health Supplement Education Act was passed, Congress intended a simple notification process for new dietary ingredients. The FDA is turning this into a pre-approval scheme, which goes against the intent of the law.

5. The FDA already has ample regulatory authority to take action against a product if it's unsafe. They don't need to have this pre-approval power, too.

6. These could be disastrous to public health. At a time when preventative measures are even more important to health care costs, the FDA is limiting access to preventative health care.

7. The cost of complying with these guidelines would be astronomical. Experts estimate that the studies required would cost between $100,000 and $200,000 per ingredient notification. That adds up to millions of dollars per supplement company. Smaller companies would not be able to afford this and would go out of business.


The economy is already hurting and we have high unemployment. Experts estimate that this could cost the economy tens of billions of dollars and result in the loss of tens of thousands of jobs.

8. The government's resources are already stretched. We have record budget deficits and record debt. Why enact more regulations when there are no safety issues here?

* I request that Congress direct the FDA to carefully review their draft guidance. If they do not amend the guidance to reflect my concerns, I request that Congress call hearings at the end of the review process. I also call on Congress to write legislation that would "grandfather" all supplements currently on the market.

* Thank you for your time.




After the phone call, send a letter to your senators and reps, making the same points. Make sure the letter is in your own words (form letters tend not to work as well). You can find the e-mail and physical addresses at the same website, http://www.usa.gov/Contact/Elected.shtml.



Then send the same letter to President Obama. (His address and phone number are on the website, too.)



Please, please, please don't make the mistake of thinking that the FDA won't take your supplements away. Similar regulations were passed in other countries, and the result was disastrous. Many supplements were taken off the market forever. In some instances, the entire supplement industry was decimated. Don't let that happen here.



Take action now! You only have a small window of opportunity to make your voice heard. Get started by going to http://www.usa.gov/Contact/Elected.shtml.