Tag Archives: medicine

Cannabis and the Constitution: A Brief History of Cannabis in the U.S.

Lisa Rough

The Constitution of the United States is arguably the most important document in the history of this country, aside from possibly the Declaration of Independence. It forms the backbone of America’s most basic rights, liberties, and laws upon which democracy is founded.

In its original form, the Constitution contained no mention of drugs or alcohol. In order to enact alcohol prohibition, the Eighteenth Amendment was introduced and ratified in 1919, specifically stating that the production, transport, and sale of alcohol was illegal. The prohibition of alcohol lasted 13 years, until the Twenty-first Amendment was introduced to repeal the Eighteenth Amendment in its entirety and re-legalize alcohol.

There is no mention of cannabis, nor any other drugs, in the Constitution. Does that mean that the prohibition of cannabis is unconstitutional?

There is no mention of cannabis, nor any other drugs, in the Constitution. Does that mean that the prohibition of cannabis is unconstitutional?

The first international prohibition of drugs came in the form of the International Opium Convention, an international drug treaty commissioned in response to the rising opium trade. The International Opium Convention was signed on January 23, 1912 and went into force globally in 1919, when it was incorporated into the Treaty of Versailles. The initial objective of the treaty was not prohibition or criminalization of drugs, but rather restricting exports of opium, coca, and cannabis.

In the United States, the Pure Food and Drug Act of 1906 was the first law of its kind to deem cannabis, along with alcohol, morphine, and opium, as “addictive and/or dangerous.” The law required drug labels to list any of these ingredients, and was primarily a “truth in labeling” law, although it was credited with paving the way for the eventual creation of the Food and Drug Administration. Curiously, cannabis, cocaine, heroin, and other such drugs continued to be available legally without a prescription, so long as they were properly labeled.

Then, along came Harry Anslinger.

RELATED STORY

The Origin of the Word ‘Marijuana’

As head of the Federal Bureau of Narcotics, Anslinger took note of the rising use of cannabis in the 1930’s. In 1935, he urged Franklin D. Roosevelt to adopt the Uniform State Narcotic Act, using the Hearst newspaper chain to promote the campaign. The Uniform State Act defined “habit forming drugs” as coca leaves, opium, “cannabis indica,” or “cannabis sativa,” and although only nine states adopted the regulations, it was drafted without any scientific study or evidentiary basis for the marijuana section.

Anslinger continued on a nationwide campaign against cannabis, declaring that marijuana causes temporary insanity. He produced films and advertisements that featured young people smoking cannabis, committing crimes, and killing themselves or others. This is exemplified in the infamous propaganda film, Reefer Madness.

The U.S. government official also made no compunctions about who, exactly, the campaign was aimed against. “Reefer makes darkies think they’re as good as white men,” Anslinger said. “The primary reason to outlaw marijuana is its effect on the degenerate races.” He also offered a charming portrait of the average cannabis consumer, to his knowledge. “Most are Negroes, Hispanics, Filipinos, and entertainers. Their Satanic music, jazz and swing, result from marijuana use. This marijuana causes white women to seek sexual relations with Negroes, entertainers, and any others.”

RELATED STORY

It’s Time to Treat Medical Cannabis Like Medicine

In 1937, Anslinger drafted the Marijuana Tax Act, which did not criminalize the possession or use of cannabis; rather, it imposed a tax equaling roughly one dollar on anyone commercially dealing in cannabis or hemp.

Dr. William Woodward, legislative counsel to the American Medical Association, vehemently opposed the bill, noting that much of the “evidence” presented originated from Anslinger himself, and that the use of the word “marijuana,” which was largely unknown at the time, prevented physicians from realizing they would lose cannabis as medicine. “Marijuana is not the correct term,” argued Woodward. “Yet the burden of this bill is placed heavily on the doctors and pharmacists of this country.”

Anslinger may not have actually created the law to prohibit cannabis, but he is certainly responsible for changing the public perception of cannabis from an innocuous substance available in many tinctures and medicines at the pharmacy to a dangerous, addictive, stigmatized drug, a perception that persists today.


RELATED STORY

How Mexican ‘Herbolarias’ Transformed Hemp into Psychoactive Marijuana

In 1969, Richard Nixon drafted the Controlled Substances Act, the legislation that criminalized the use and possession of cannabis, and ruled that marijuana has a high potential for abuse and no established medicinal value. The term “controlled substance” was defined to exclude alcohol and tobacco, an important exemption, as these are two of the most widely used drugs (with some of the most addictive properties).

The United States Constitution was drafted in order to spread power among many groups, by a system of checks and balances to ensure that no one person has too much power. Thus, the Controlled Substances Act could be changed by the Attorney General, the Drug Enforcement Administration, Congress, the Department of Health and Human Services, or by petition from any interested party.

Since 1970, there have been numerous petitions to reschedule cannabis. The first petition was filed by NORML in 1972 and was not given a hearing until 1986, and another attempt in 1981 from Representative Stewart McKinney was also shot down. Since then, it has been a recurrent theme of petition and denial through the years.

“Marijuana, in its natural form, is one of the safest therapeutically active substances known to man.”

Francis L. Young, DEA Administrative Law Judge

During a hearing on the subject in 1988, DEA Administrative Law Judge Francis L. Young concluded that, “In strict medical terms, marijuana is far safer than many foods we commonly consume…Marijuana, in its natural form, is one of the safest therapeutically active substances known to man.”

Whether or not the prohibition of cannabis is unconstitutional, perhaps it is time to reconsider whether the prohibition of cannabis is truly for the safety of the country, or simply for the peace of mind of a few select opponents still entrenched in the past.

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This is how the FDA can instantly criminalize any vitamin or plant extract

HEALTH FREEDOM ALERT: The FDA just outlawed CBDs and hemp oil extracts by claiming all plant molecules now belong exclusively to Big Pharma

Sunday, March 20, 2016
by Mike Adams, the Health Ranger
Tags: CBD, hemp oil extract, FDA regulations

CBD

(NaturalNews) Hemp oil extracts containing CBDs (cannibidiols) are such a threat to the pharmaceutical industry that the FDA is now invoking totally insane justifications for outlawing them.
CBDs are non-psychoactive compounds found naturally in hemp plants. They work so well as powerful natural medicine that people everywhere are realizing CBDs work better than pharmaceuticals for treating epilepsy, seizures, neurological disorders and other serious health conditions (including HIV infections).
So the FDA has just launched a massive regulatory assault against CBDs by invoking the most insane logic you’ve ever heard. Here’s how it goes:
1) CBDs work so well that drug companies are now investigating them to be approved by the FDA as medicines.
2) Because CBDs are being investigated by drug companies, the FDA has granted CBDs status as being “investigated as a new drug.” In the FDA’s own language from their website, “FDA considers a substance to be ‘authorized for investigation as a new drug’ if it is the subject of an Investigational New Drug application (IND) that has gone into effect.”
3) Because CBDs work so well and have been authorized for drug investigations, the FDA now OUTLAWS them being sold as dietary supplements. Per the FDA’s own website: “FDA has concluded that cannabidiol products are excluded from the dietary supplement definition under section 201(ff)(3)(B)(ii) of the FD&C Act. Under that provision, if a substance (such as cannabidiol) has been authorized for investigation as a new drug for which substantial clinical investigations have been instituted and for which the existence of such investigations has been made public, then products containing that substance are outside the definition of a dietary supplement.”
4) Now the FDA has begun sending warning letters to CBD makers, claiming they are in violation of FDA regulations because they are selling “adulterated products.” Adulterated with what, exactly? CBDs, of course! “The debate over hemp CBD’s legal status continues after FDA sent eight warning letters to manufacturers of CBD dietary supplement and food products earlier this month,” reports Nutritional Outlook. “The warning letters cite impermissible health claims used to market the products, as well as CBD’s invalid status as a dietary ingredient due to its presence in two drug applications currently under consideration.”

The FDA just criminalized one of the most miraculous healing medicines in the world by handing it over to Big Pharma

In other words, the FDA just handed Big Pharma an absolute monopoly over CBDs (hemp oil extract) by ridiculously claiming such natural products are “adulterated” with molecules (CBDs) that the FDA says might one day become a drug.
“Drugs,” according to the FDA, are substances that are proven to treat, prevent or cure a disease, and thus the FDA’s own logic admits that CBDs must be able to treat, prevent or cure diseases, otherwise they would be useless as “drugs”.
But when a dietary supplement company makes the same claim, they are hit with aggressive warning letters from the FDA, threatening to shut them down, confiscate their products and seek criminal prosecution of the company executives.

This is how the FDA can instantly criminalize any vitamin or plant extract

Do you see how this twisted, corrupt regulatory tactic can allow the FDA to instantly criminalize any dietary supplement, vitamin, herb or plant extract?
Vitamin D, for example, could be outlawed by the FDA announcing that it has granted “Investigational New Drug application (IND)” status to any drug company studying vitamin D.
Using this same corrupt, mafia-style tactic, the FDA could outlaw resveratrol or even vitamin C, denying Americans the right to access safe, affordable, natural substances that are routinely found in nature.

It’s time to end the FDA’s monopolization over natural plant molecules

If humanity is ever to achieve medical freedom, we must end the FDA’s outrageous medical monopolization of plant molecules such as CBDs. By allowing this corrupt, criminally-run regulatory agency to criminalize every molecule found in nature, our nation’s lawmakers condemn us all to life in what can only be called medical totalitarianism under FDA tyranny.
Any time a healing substances is found in nature, the FDA can simply assert that such molecules are now in the process of being studied as drugs and are therefore illegal to sell as dietary supplements even though they were developed by Mother Nature, not drug companies.
This FDA tactic is nothing more than the FDA proclaiming intellectual monopolies over all molecules of interest found in nature. It is Monsanto-like in its arrogance and wickedness, and it deprives the People of their right to access medicinal plants and healing substances that have existed in nature for countless thousands of years long before the FDA ever came into existence (1906).
If we do not stop this FDA, we are all doomed to living under a totalitarian regulatory regime that will systematically criminalize every healing molecule found in nature, from the curcuminoids in turmeric root to green tea catechins and even phycocyanins found in spirulina.
That this federal agency has now resorted to such tactics of medical totalitarianism and outright tyranny is proof that we need to strip the FDA of regulatory powers over natural dietary supplements and limit its domain to pharmaceutical drugs only.
Coincidentally, a Presidential election is upon us that threatens to shake up the entire establishment if the right person wins. “Establishment” candidates on both sides of the aisle would simply continue the FDA war on natural molecules that’s now under way, but there is one candidate who has openly threatened to challenge the authority of federal regulators like the EPA and FDA.

FDA begins crackdown by targeting inaccurate label claims… but it won’t end there

The FDA has now declared war on CBDs and hemp oil extracts. Its first targets are those companies who have inaccurate label claims or are committing outright fraud in claiming CBD concentrations that don’t even exist in their products.
On this point, I must agree that inaccurate label claims deserve regulatory enforcement. The CBD industry is heavily populated with fraudulent sellers whose products often contain no CBDs at all.
“The FDA has turned its back on the cannabis industry, claiming that CBD products cannot be sold as dietary supplements,” reports Canna Business. “Companies affected by the latest crackdown include Cali Stores, Dose of Nature, Green Garden Gold, Healthy Hemp Oil, Michigan Herbal Remedies, Morgue Juice, Pain Bomb and Sana Te Premium Oils. According to the FDA’s analysis, all products contained different amounts of 9-THC, THCa, CBDa, CBN and CBD than they had claimed.”
The second target of the FDA is companies that made disease treatment claims that their CBD products might treat epilepsy, cancer or other conditions. The FDA, of course, routinely attacks any dietary supplement maker that tells the truth about the medicinal benefits of their products. According to the FDA, there is no such thing as any food, nutrient, herb or natural molecule that has any ability whatsoever to treat, prevent or cure any disease. This position is, of course, patently absurd and stands in total violation of nutritional science, but it is the “big lie” the FDA must maintain in order to keep putting dietary supplement companies out of business.
Once the FDA finishes destroying all the companies with inaccurate labels and disease marketing claims, it will target all the honest suppliers of CBDs who are selling genuine, honest products that contain accurate CBD labels. This is the real goal of the FDA: to threaten, intimidate and destroy the entire CBD industry and thereby protect the medical monopolies of drug companies that can’t wait to cash in on these amazing molecules that really do treat disease (otherwise, Big Pharma would have no interest in them).

This is how the FDA keeps the medical racket marching along

And so the great medical monopoly racket marches on, with the FDA giving a big “F-YOU” to the American people while handing lucrative medical monopolies to its greed-driven friends in the pharmaceutical industry. Meanwhile, the American people are denied healing medicine that works at a fraction of the cost of overpriced pharmaceuticals.
Entrepreneurial companies that offer such hemp oil extracts containing CBDs — natural medicines that could help reduce human suffering while lowering health care costs nationwide — are threatened by the FDA with devastating enforcement actions that could land their executives in prison.
This is all part of the FDA’s war on natural medicine that systematically criminalizes molecules found in nature and the people who seek to make those molecules available to patients in need. While disease suffering skyrockets across America and medical expenses push more and more families over the threshold of bankruptcy and destitution, isn’t it comforting to know that your federal government is doing everything in its power to deny you access to safe, affordable natural medicine while protecting the profits of the drug giants?

What can you do to oppose this medical tyranny by the FDA?

None of this is ever going to change, by the way, if we keep electing establishment politicians to the White House. If you want to see real change in the legalization of hemp extract components such as CBDs, you’d better vote for someone who terrifies the establishment and threatens to tear it down.
At the same time, you need to support health freedom organizations like the Alliance for Natural Health, which is fighting to keep dietary supplements legal in America.
You should also watch this video animation that exposes the anti-dietary supplement bias of PBS Frontline, which recently ran a totally dishonest hit piece documentary attacking supplements.
There is a nationwide effort under way right now to criminalize ALL dietary supplements and force every plant extract, vitamin or food concentrate to be regulated by the FDA as if they were prescription drugs. This would utterly wipe out the entire dietary supplements industry and plunge America into an era of runaway disease, suffering and death as people are denying access to the healing nutrients that are presently preventing disease (and even reversing serious disease in some cases).
Finally, share this story and join the Natural News email list (below) to stay informed on all this. As the editor of Natural News, I am fighting for your right to access CBDs and hemp oil extracts, as they are amazing natural medicines that can treat, prevent and in some cases even help cure serious health conditions.

The FDA is anti science and anti human rights

We have a fundamental human right to access healing plants found in nature, and the FDA has systematically sought to destroy that right and criminalize those who seek to express it. Access to Mother Nature’s healing molecules is a fundamental human right that exists above and beyond the Bill of Rights. It is a DIVINE right.
To reestablish our access to these rights, we need a political revolution in Washington that puts people in power who are ready and willing to dismantle the FDA and end its devastating monopolies over dietary supplements, medicinal herbs and natural molecules found in nature.
We need to legalize health freedom in America and set this nation on a new path of disease prevention and drastically reduced health care costs through access to affordable, natural medicines. The only way to accomplish this is to end the FDA’s reign of tyranny over the dietary supplements industry.
We need a new health freedom revolution in America, and it starts at the ballot box. It’s time to start electing outsiders, not insiders… people who the terrify the Washington establishment because they know their insidious grip on regulatory power will be challenged. If you want medical marijuana legalized, or if you want access to CBD oil as an affordable dietary supplement, it’s time to start voting for people the establishment is desperately trying to destroy. Because it is only those people who have any real hope of achieving the kind of political and legislative goals that will end the FDA’s stranglehold on natural medicine in America.

Food Forensics: Breakthrough book from the Health Ranger exposes shocking scientific truth about what you’re really eating

Over two years in the making, Food Forensics publishes the heavy metals testing results from over 800 foods, supplements, spices and superfoods. Available now for pre-order on Amazon and BN, click here for the Food Forensics website and book preorder links. “An amazing job on so many levels and an absolute must read.” – Michael T. Murray… “Mike Adams new book, Food Forensics, should be required reading for all the Big Food, Big Biotech apologists who continue to poison and mislead us.” – Ronnie Cummins, Organic Consumers Association … “Food Forensics is an essential reality guide to food and water in the 21st century.” – Robert Scott Bell … “Food Forensics is an incredible, ground-breaking book.” – Ty Bollinger, The Truth About Cancer …
Click here to preorder your copy of “Food Forensics” now.
Sources for this article include:
http://www.fda.gov/NewsEvents/PublicHealthFo…
http://www.nutritionaloutlook.com/herbs-bota…
http://www.cannabusiness.com/news/products-i…

Learn more: http://www.naturalnews.com/053369_CBD_hemp_oil_extract_FDA_regulations.html#ixzz43aLcL8Km

Declaration on Seed Freedom

  1. Seed is the source of life, it is the self urge of life to express itself, to renew itself, to multiply, to evolve in perpetuity in freedom.
  2. Seed is the embodiment of bio cultural diversity. It contains millions of years of biological and cultural evolution of the past, and the potential of millennia of a future unfolding.
  3. Seed Freedom is the birth right of every form of life and is the basis for the protection of biodiversity.
  4. Seed Freedom is the birth right of every farmer and food producer. Farmers rights to save, exchange, evolve, breed, sell seed is at the heart of Seed Freedom. When this freedom is taken away farmers get trapped in debt and in extreme cases commit suicide.
  5. Seed Freedom is the basis of Food Freedom, since seed is the first link in the food chain.
  6. Seed Freedom is threatened by patents on seed, which create seed monopolies and make it illegal for farmers to save and exchange seed. Patents on seed are ethically and ecologically unjustified because patents are exclusive rights granted for an invention. Seed is not an invention. Life is not an invention.
  7. Seed Freedom of diverse cultures is threatened by Biopiracy and the patenting of indigenous knowledge and biodiversity. Biopiracy is not innovation – it is theft.
  8. Seed Freedom is threatened by genetically engineered seeds, which are contaminating our farms, thus closing the option for GMO-free food for all. Seed Freedom of farmers is threatened when after contaminating our crops, corporations sue farmer for “stealing their property”.
  9. Seed Freedom is threatened by the deliberate transformation of the seed from a renewable self generative resource to a non renewable patented commodity. The most extreme case of non renewable seed is the “Terminator Technology” developed with aim to create sterile seed.
  10. We commit ourselves to defending seed freedom as the freedom of diverse species to evolve; as the freedom of human communities to reclaim open source seed as a commons.

To this end, we will save seed, we will create community seed banks and seed libraries, we will not recognize any law that illegitimately makes seed the private property of corporations. We will stop the patents on seed.


Click here to sign the declaration

Click here to download a PDF

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Marijuana is medicine, Journal of the American Medical Association concludes

Posted on June 23, 2015 at 10:06 am by David Downs in featured, Health, Science

li-620-marijuanagrow

Marijuana is one hundred percent a form of medicine, researchers conclude in a bombshell series of reports released today by the Journal of the American Medical Association.

Cannabis — which has been used medicinally for thousands of years — reduces nausea, and vomiting, and pain, as well as spasticity, a panel of researchers conclude, after reviewing a total of 79 trials.

“Use of marijuana for chronic pain, neuropathic pain, and spasticity due to multiple sclerosis is supported by high-quality evidence,” one of the reports found.

Researchers bemoaned the lack of high-quality trials of marijuana. That situation that can be laid at the feet of cannabis prohibition. The federal government maintains cannabis is a highly dangerous drug with no medical use. Researchers must cut through more red tape to research a pot plant than any other substance on the planet, doctors say.

However, this week, the federal government slightly reduced the regulatory hurdles to study cannabis — down from eight layers of review, to seven.

More than 750,000 Americans will be arrested for cannabis this year.

The Obama administration has spent an estimated $300 million interfering with state medical marijuana programs and patients, including arresting and prosecuting patients and caregivers. Thirty-five states have medical cannabis laws, and some members of Congress are working to de-fund federal attacks on medical marijuana.

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In Siberia charred seeds have been found inside burial mounds dating back to 3000 B.C.

Picture of

 

By Hampton Sides

Photographs by Lynn Johnson

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There’s nothing new about cannabis, of course. It’s been around humankind pretty much forever.

In Siberia charred seeds have been found inside burial mounds dating back to 3000 B.C. The Chinese were using cannabis as a medicine thousands of years ago. Marijuana is deeply American too—as American as George Washington, who grew hemp at Mount Vernon. For most of the country’s history, cannabis was legal, commonly found in tinctures and extracts.

Then came Reefer Madness. Marijuana, the Assassin of Youth. The Killer Weed. The Gateway Drug. For nearly 70 years the plant went into hiding, and medical research largely stopped. In 1970 the federal government made it even harder to study marijuana, classifying it as a Schedule I drug—a dangerous substance with no valid medical purpose and a high potential for abuse, in the same category as heroin. In America most people expanding knowledge about cannabis were by definition criminals.

But now, as more and more people are turning to the drug to treat ailments, the science of cannabis is experiencing a rebirth. We’re finding surprises, and possibly miracles, concealed inside this once forbidden plant. Although marijuana is still classified as a Schedule I drug, Vivek Murthy, the U.S. surgeon general, recently expressed interest in what science will learn about marijuana, noting that preliminary data show that “for certain medical conditions and symptoms” it can be “helpful.”

In 23 states and the District of Columbia cannabis is legal for some medical uses, and a majority of Americans favor legalization for recreational use. Other countries are rethinking their relationship to pot too. Uruguay has voted to legalize it. Portugal has decriminalized it. Israel, Canada, and the Netherlands have medical marijuana programs, and in recent years numerous countries have liberalized possession laws.

Ganja is simply around us more, its unmistakable but increasingly unremarkable smell hanging in the air. Yes, smoking it may lead to temporary laughing sickness, intense shoe-gazing, amnesia about what happened two seconds ago, and a ravenous yearning for Cheez Doodles. Though there’s never been a death reported from an overdose, marijuana—especially today’s stout iterations—is also a powerful and in some circumstances harmful drug.

Still, for many, cannabis has become a tonic to dull pain, aid sleep, stimulate appetite, buffer life’s thumps and shocks. Pot’s champions say it peels back layers of stress. It’s also thought to be useful as, among other things, an analgesic, an antiemetic, a bronchodilator, and an anti-inflammatory. It’s even been found to help cure a bad case of the hiccups. Compounds in the plant, some scientists contend, may help the body regulate vital functions—such as protecting the brain against trauma, boosting the immune system, and aiding in “memory extinction” after catastrophic events.

In the apparent rush to accept weed into the mainstream, to tax and regulate it, to legitimize and commodify it, important questions arise. What’s going on inside this plant? How does marijuana really affect our bodies and our brains? What might the chemicals in it tell us about how our neurological systems function? Could those chemicals lead us to beneficial new pharmaceuticals?

If cannabis has something to tell us, what’s it saying?

PLEASE CONTINUE READING…..

Make the FDA Advisory, Not Mandatory

You should control what medicines you use, not the FDA. The FDA should make advisory recommendations only. It should NOT have the power to mandate which drugs you can buy, and which you cannot.

  • If pharmaceutical companies value the FDA seal of approval, then they can pay the FDA to evaluate their drugs.
  • If consumers value FDA approval, then they can decide to only buy FDA approved drugs.

If the FDA’s seal of approval is really so valuable, then it does NOT need to be mandatory. No coercion is necessary. Instead, the FDA should be able to sell its services through voluntary means, just like Underwriter’s Laboratory does.

Consumers and doctors should be free to consult available science, and make their own decisions about which treatments to try.

All human beings are unique. Treatments that might be dangerous for one person, could be the only possible solution for another. There is zero chance that one-size-fits-all dictates can possibly account for the vastness of human variability. Patients and doctors must have the flexibility to deal with individual human uniqueness.

The FDA should serve, not rule.

Talking Points:

There are thousands of reasons why the FDA should lose its power to coerce you and your loved ones. Some of these reasons will be listed below, so that you can use them when writing to Congress, or when asking your friends to contact Congress on this issue . . .

The FDA gives consumers a false sense of security. Americans assume that the FDA is actually protecting them, but it is not. For instance . . .

The Union of Concerned Scientists surveyed 6,000 FDA scientists in 2006, and 1,000 of them responded with the following disturbing admissions:

  • 17% admitted that they had been "asked explicitly by FDA decision makers to provide incomplete, inaccurate, or misleading information to the public, regulated industry, media, or elected/senior government officials."
  • Less than half agreed that the FDA "routinely provides complete and accurate information to the public."
  • 47% admitted to being aware of instances "where commercial interests have inappropriately induced or attempted to induce the reversal, withdrawal, or modification of FDA determinations of actions."

The FDA is constantly attempting to expand its powers. The people in that agency are relentlessly pushing into areas that are NOT part of their mandate — even where there is NO problem that needs to be fixed.

For Example: The FDA has made repeated attempts to regulate vitamins and supplements, even though there is no evidence that these things present any danger. Quite the contrary — vitamins and supplements are a powerful example of how health outcomes can be improved, without FDA involvement. The website of the Life Extension Foundation is full of scientific citations to demonstrate this. For instance . . .

A review of 2009 information for "adverse events" reported to the national control center’s data system shows that, NO major adverse events or deaths were reported for . . .

  • Botanical supplements like St. John’s wort, ginseng, and Echinacea
  • Hormone supplements like DHEA, melatonin, and pregnenolone
  • Phytoestrogen supplements
  • The joint- and cartilage-support supplements glucosamine and chondroitin
  • Vitamins A and E, and only one adverse event each was reported for vitamin B6 and C

In total, 41 major adverse events were reported for the entire spectrum of supplements including botanicals, amino acids, and vitamins, and only one was a death.

In contrast, more than 7,000 major adverse events were reported for pharmaceutical drugs, including a total of 496 deaths. And based on previous studies, we know the overall death rate for physician prescribed drugs to be far higher.

The Downsize DC position is pro-choice. The FDA should serve, not rule.

Use the form at right to send your elected representatives a letter about this issue. It’s easy!

  • Your position will be counted by each Congressional office,
  • Will educate the Congressional staffer who reads it,
  • May be passed up the chain of command,
  • May receive a reply (many DC Downsizers get them). If you receive such a letter, please share it with us at Comments@DownsizeDC.org.

 

Send a letter to Congress

We provide the first few words of the letter so that Congressional offices will see the most important point

right at the start, and so that no one can hijack our system for another purpose.

Here’s the part we provide . . .

Make the FDA advisory, not mandatory.

LINK

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