May 24, 2007

FDA's new CAM guidelines . Mike Adams comments

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Originally published May 23 2007



Even I can read between the lines on this one with my eyes CLOSED.

There are many EXCELLENT healing agents on this planet NOT made by Big Pharma - how many are going to be left for us to use ...?




Read between the lines on the FDA's CAM Guidelines






by Mike Adams



If you've been following the debate over the FDA's new CAM Guidelines

that threaten to destroy natural medicine by regulating herbs,

supplements and even vegetable juices as


"unapproved drugs," you've no doubt heard the opposing opinion by some natural

health commentators who claim the guidelines say nothing new. Some are

even saying the CAM Guidelines are a "non issue" and represent "no big

deal."



As much as I appreciate the efforts and comments of others in the

natural health world, I strongly disagree with their assessment on the CAM

Guidelines. Here's why: Their assessment of the threat of the CAM

Guidelines is based on a fatal flaw -- the assumption that the FDA will only

look at these guidelines as a theoretical document and not take direct

action on them. And as we've all seen, once guidelines are translated

into action by any governmental organization, they immediately undergo

an expansion that takes their application far beyond whatever original

intent was written in the document.



For example, when the RICO Act was initially passed (Racketeer

Influenced and Corrupt Organization Act) in 1970, lawmakers insisted it would

only apply to organized crime gangs. You know: mob bosses and their

henchmen. But guess what? The term "Corrupt Organization" has been expanded

to mean almost anything, and now the RICO Act is being applied against

corporations, industry trade groups and even police departments!

(Deservedly so, no doubt, but still far outside the original idea of the

law.)



When the Patriot Act was frantically passed by a terrified nation in

2001, it was loudly proclaimed the Act would only target "terrorists."

But guess what? The Patriot Act has been used against American citizens

engaging in petty crimes. It has even been used to label animal rights

activists "terrorists" for merely attending meetings that sought to free

animals from corporate torture experiments (testing cosmetics,

chemicals and the like).



I'm fairly certain that when lawmakers signed the Patriot Act, they

weren't thinking of abortion rights protestors and animal rights

activists, but laws have a way of expanding their scope far beyond their

original intent. Thanks to the Patriot Act, the very act of sitting in a room

with a friend and discussing the evils of the American government can

get you labeled a terrorist engaged in a conspiracy (if anyone happens

to be listening, of course).



Now let's consider the FDA's CAM Guidelines in which the agency states

it could regulate vegetable juice as a drug as long as the juice is

sold with the intent to improve health. The document specifically mentions

massage oils and herbs as being subject to regulation, too. If this

becomes adopted as the primary regulatory philosophy by the agency, the

application of this thinking will inevitably expand.



Today, the FDA says it won't be attacking natural health clinics,

breaking down doors with armed agents and arresting the healers inside. The

quiet, behind-closed-doors practice of using medicinal herbs,

homeopathic remedies, nutritional supplements or even Bach Flower Remedies will

be tolerated... for now.



But then, one day a new tyrant will lead the FDA, and he (it's always a

HE) will interpret the CAM Guidelines in a new way. He'll say the

guidelines clearly spell out that the FDA should be regulating ALL

naturopathic remedies in order to "protect consumers." And he could unleash a

new wave of medical tyranny, reauthorizing the SWAT-style FDA raids we

saw in the 1980's and 1990's, all while claiming the CAM Guidelines

document blazed the trail by spelling out specific examples of what needed

to be done.



Just like the RICO Act and the Patriot Act, the FDA's CAM Guidelines

could one day exceed their intended purpose and be used against Americans

in ways we never imagined possible.



How do you boil a frog?Those commentators in the natural health

movement who are telling you there's nothing to worry about here are

regretfully failing to see where this is all headed. The FDA, you see, is

smart enough to know it can't just announce a massive, sweeping ban of

everything in the world of natural medicine. Too many people would march in

the streets. So it has to first test the waters with a "line of

thinking" document in order to gauge the public reaction. That's the real

purpose of the CAM Guidelines document. It's really just a test to see if

anybody's paying attention.



If that passes muster and the public outcry isn't too loud, the next

step is to start issuing regulations and taking actions based on that

line of thinking. The FDA might increase the number of threatening legal

letters sent to supplement companies or raw juice fasting retreats. They

might even conduct a raid on some easy target (like the "Cocaine"

energy drink company) to see if the public can stomach that sort of

aggression action. With each action, they are testing the waters to see if they

can get away with yet another expansion of their power.



They undermine your health freedom the same way you boil a frog: Put it

in a pot of room temperature water, then crank up the heat slowly. By

the time the frog realizes he's being cooked, he's too close to dead to

jump out. This is the sort of health freedom trap being set for the

American people by the FDA. And those who say this is all no big deal are

essentially treating you all like frogs and saying, "Come on it, the

water's fine!"



Don't be fooled. If the FDA wasn't trying to test the waters with

something new, there would be no reason to issue the CAM Guidelines in the

first place. Those comments from organizations and individuals in the

natural health industry who are saying there's "nothing new" in these

guidelines are ignoring the primary tactic being used by the FDA. The FDA

is laying the groundwork to censor or regulate every substance used in

natural medicine, and the CAM Guidelines document is a "playbook" that

reveals how this might unfold.




This is how it's done by arrogant government departments: Float an idea

piece, write regulations, then start applying those regulations until

they become accepted as "the way things are done." At each step, the FDA

is gauging the public reaction, or even trying to slip it all under the

radar so they can later claim something like, "Nobody complained

before!"



Learn to read between the linesFriends, we've all got to operate as

critical thinkers today. You can't just take these documents at face

value and think the FDA is going to abide by the letter of the law. It's

important to ask youself, Where is the FDA going with this? Why did they

go to the trouble to float this document?



Think about where this is heading. Why would they spell out the example

of regulating vegetable juice if they didn't plan to someday enforce

such regulatory ideas? The FDA has already proven it is the enemy of

health freedom. It is entirely consistent with the agency's past behavior

to believe it will continue to march towards banning, censoring or

regulating out of existence any substance that competes with pharmaceutical

profits.



The CAM Guidelines spell it all out, plain as day. Reading between the

lines on this one isn't even very difficult. And I dare say that only a

fool would believe the FDA feels any obligation whatsoever towards

protecting the health of the public.



It's the same story with the Reagan-Udall Foundation.  Also recently

passed by the U.S. Senate is a bill that would "revitalize" the FDA and

create a Reagan-Udall Foundation for the Food and Drug Administration

that could earn royalties licensing drugs or medical devices. Depending on

whom you ask, the creation of this foundation either puts the FDA in

business with Big Pharma, or is "no big deal" and has nothing to do with

licensing drugs or medical devices.



Once again, I remind readers to read between the lines. At its

inception, the Reagan-Udall Foundation may, indeed, not pursue the licensing of

drugs, but its activities will inevitably expand into areas not covered

in the original language of the law. It is naive to believe that any

governmental organization will simply halt when it reaches the boundary

of whatever power has been granted to it. All governments and government

organizations seek to expand their power. It is a natural law of

bureaucracy.



Want the ultimate example? The entire U.S. government was supposed to

be operating on power granted to it by the people. The U.S. Constitution

specifically said that all powers NOT granted to the federal government

are reserved to the people (the States). But look around you. Do you

see a government that feels it owes its power to the people? Do you see a

government that humbly serves the people, or that keeps its hands off

powers not directly granted to it by the Constitution? Not a chance. Our

government RULES the people. It has take the power granted to it by the

U.S. Constitution and expanded it into an empire that now rules over

the very people it was supposed to serve.



Government power always expands just as sure as sewage runs downhill.





For anyone to believe that the FDA (or its foundation) will refrain from

engaging in its own expanding power grab is remarkably naive. Be

warned: The FDA's CAM Guidelines are a blueprint for increased FDA typranny

over the people, and a game plan for destroying alternative medicine.

---------------------------------



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