THE VACCINE NATION

 

THE VACCINE NATION

 

by Jon Rappoport

 

MARCH 10, 2012. Well, it’s actually vaccine world.

 

Anyway, let’s start here. In my new collection, THE MATRIX REVEALED, I print many interviews with a retired propaganda operative, Ellis Medavoy (pseudonym). Ellis is the very best authority I’ve ever found on the subject of media deception and how that game actually works. The nuts and bolts. The cultivating of “reliable sources” who lie to reporters night and day. The spreading of false medical information. The strategies for building a long-term propaganda campaign. The subtle and not-so-subtle methods of hypnotizing the public consciousness. It’s PhD stuff you can’t obtain in a university.

 

In a conversation about so-called epidemics and pandemics, Ellis handed me this nugget:

 

Look, there will be one phony epidemic after another. You already know that. You’ve ferreted out the statistics. On the one hand, these non-epidemics are pumped up and promoted to convince people they must get vaccinated. On another level, the promotion is for the purpose of conditioning people to accept any and all medical advice, to drag them into the system.

 

But here’s what you’re missing. People like me know, up front, that these scare-promotions could very well fail. Because the public is, unfortunately, smarter than we often give them credit for. They’ll decide not to get vaccinated. But you see, I don’t care about that. Because it’s all about cost-benefit analysis. Do you see? What does it cost to promote an epidemic that isn’t an epidemic? And what are the LONG-TERM benefits of doing that? How many people who REFUSE THE VACCINE are nevertheless tipped and tilted a little bit toward accepting, in general, the authoritarian medical religion? How many people are, essentially, hypnotized JUST A LITTLE BIT in the direction of surrendering their freedom to medical dictates?

 

When I was working full-bore in this area, that’s the way I thought about things, because I knew there would be many, many medical propaganda campaigns over the course of many years. And I also knew that, all in all, they would bear fruit. They would wear people down. And that was my goal. To finally, on that last day, get someone to say, ‘All right, I give up. The authorities must be right.’

 

That’s what I worked for. That day. That moment. The payoff. You have to pace yourself for the long haul. You have to accept losses and look to the future. Outfits like the Centers for Disease Control and the World Health Organization are trying to get people to accept their falsehoods right now. That’s their job. That’s all they know. People like me didn’t think in those terms.

 

Really, a major part of propaganda should involve changing the RHYTHMS of the mind. You want to establish certain HARMONIES in the mind that add up to acceptance…”

 

I was struck by Ellis’ words, because I had known a few people who were very intelligent and very skeptical, people who had been diagnosed with one thing or another, who were still healthy, who had refused to take a medical drug that was prescribed for them. I had seen them, over a period of years, slowly gravitate toward the Priest in the White Coat, slowly believe published studies I knew to be false, slowly give in and finally take that drug—and THEN THEY HAD GOTTEN SICK AND DIED.

 

Ellis and I had a number of conversations about THAT, and he told me it was one reason he finally retired from the game. He has a lot to feel guilty about and he knows it. He doesn’t ask for forgiveness and I don’t offer it. Just the way you wouldn’t offer forgiveness to a president who sent men and women to die in a war that wasn’t necessary.

 

Okay. With that as background, let’s move ahead.

 

I’ve written many articles about the so-called outbreaks, epidemics, and pandemics of the last 25 years—SARS, bird flu, West Nile, Swine Flu… The stats show these illnesses, at best, were duds. They never spread to a fraction of the extent predicted.

 

And was there ever prediction! Everybody and his cousin got in on the act. Doctors, public health agencies, political leaders, conspiracy researchers. Frankly, to blow my own horn a little, I was one of the people who put this crap to bed. I raked the fear mongers over the coals and showed, from a number of angles, why the predictions were based on no firm evidence at all.

 

But the mainstream epidemic mongers did accomplish one goal. They took the opportunity to hammer the global population over the head with the idea that WE ALL MUST GET VACCINATED.

 

In some countries, alas for them, it didn’t work. People caught on the to the basic scam.

 

However, the PR never stops. In one small example, the governor of Washington state, last year, signed into a law a measure that makes it mandatory for parents (who want to opt out of vaccinating their kids) to first visit a health practitioner, who is now duty bound to provide information about vaccines. This doctor’s appointment has to precede a parent’s decision to claim a religious or philosophical exemption from vaccines for her child.

 

The medical strategy is to keep up relentless repetition about the need for and value of vaccination—and these fake epidemics provide the opportunity in spades.

 

The PR campaign also provides citizens, who think they’re quasi-doctors and scientific elitists, with the chance to spout off about vaccination as a duty of every responsible parent. Typical boomer nonsense.

 

However, it does work, because peer pressure is a strong force—and so parents who are on the outside looking in, and don’t want to vaccinate their kids, are thought of as crazies. Dangerous crazies, who are exposing their own children, and other children in the community, to illness.

 

Many PR campaigns have this component. They may not succeed in all their goals, but they do define two basic groups—the normals and the nuts.

 

The normals (android types) look at the nuts and build up resentment toward them. And the nuts feel oppressed.

 

It’s called a squeeze play.

 

During the centuries of Roman Church domination, it was called excommunication.

 

From a purely political angle, it’s quite ingenious, this vaccine promotion…because it pretends that, without all the shots, whole populations will fall under the gun of communicable disease and we will all revert back to darker times.

 

I’ve spent many hours writing and talking about this false premise—how the decline of infectious disease in the West was the result of non-medical factors: basic sanitation, elimination of overcrowding, the rise of the middle class, and improved nutrition. (See Ivan Illich’s groundbreaking classic, Medical Nemesis.)

 

The vaccination PR campaign has the objective of making everyone into a Group. One big group. All of humanity. Interdependent. The Global Village. That’s the vector of attack against our freedom to choose, to vaccinate or not:

 

No, you can’t do that. You’re part of everyone else, and if you don’t follow our vaccine directives, you’re endangering the collective.”

 

This is why, for the last 23 years, I’ve been educating people about the fact that medical propaganda and enforcement are the very best method for attaining long-range political control. The propaganda has no apparent partisan slant. It seems to favor no political cause at all. It has a neutral concerned scientific attitude. Along with, of course, the notion that the experts know everything and we, the children, know nothing.

 

And since we know nothing, we have no right to exercise our freedom to choose. That freedom stops at the door of “science.”

 

If you believe that one, you’re cooked. They’ve got you.

 

Look up the road into the future. Use a little common sense and a little imagination, and you’ll be able to see where this is heading. Unless it’s derailed.

 

I’m betting it’s not a place you want to be.

 

That’s why freedom matters.

 

I know, freedom is now a dirty word. Well, that’s the result of a whole other propaganda op.

 

They’re connected, believe me. The medical cartel and political collectivism. They’re together on an elite chessboard.

 

Two streams coming together.

 

Here are the best official statistics I could dig up for the phony epidemics I’ve been talking about. These numbers are global, and cumulative:

 

SARS: 774 deaths.

WEST NILE: 1,088 deaths

BIRD FLU: 262 deaths

SWINE FLU (H1N1): 25,000 deaths.

 

Keep in mind that the CDC claims ordinary seasonal flu in the US kills 36,000 people a year, and the World Health Organization states that ordinary seasonal flu kills between 300,000 and 500,000 people a year, globally. NONE of that is called an epidemic.

 

Quite interesting. Quite instructive. What it tells you is this: the phony epidemics are largely PR and propaganda campaigns. They’re launched and funded and maintained to condition people to Medical Authority. Operant conditioning, mind control, brainwashing.

 

However, the wild card in all this is the Internet. During the last go-around with Swine Flu, there were enough of us who blew the whistle on the CDC and the World Health Organization to derail the whole operation. Governments and their medical partners were screaming and ranting and lying on every front, and it didn’t work. We exposed their lies, chapter and verse. We demonstrated that the “level-six pandemic” was a fraud.

 

The non-official media won.

 

Millions of people started to wake up from their trance.

 

So now the medical/government honchos don’t know what to do. They want to launch another phony epidemic, and I’m sure they will. But they don’t know how to promote it. They’re gagging on their own lies. They’re searching for newer and better methods of propaganda.

 

The vaccine manufacturers are furious. They struck a deal some years ago with governments that would allow them to keep making vaccines at a high rate of profit, sell those vaccines to governments with a no-return policy, and avoid huge lawsuits when people who took the vaccines died…they were riding high. But now?

 

The governments and their propaganda machines didn’t deliver. They fell down on the job. They lost the information war. To us. And now we’re ready to pounce on the next load of insanity and de-certify it. We know where the lies are. We can expose them.

 

This is a model to emulate in other venues. Other issues can be dealt with in this way.

 

When Swine Flu was birthed in La Gloria, Mexico, on a huge commercial pig farm in 2009, it was assumed the whole world would eventually line up and dutifully take a jab of vaccine.

 

Of course, what happened on that pig farm was simple. There were, to use a mainstream-media phrase, feces lagoons everywhere. Pig feces. In the open air. And workers were getting sick. Sure they were getting sick, because that’s precisely the kind of environment where people DO get sick. It isn’t one germ, it’s the whole setting. Live in tons of rotting waste for a long time and you WILL get sick.

 

And then outside contractors came in and sprayed all sorts of toxic chemicals on the lagoons—and more people got sick. No big surprise there, either.

 

And then, guess what? The CDC sent a team of researchers down to La Gloria to find out what was making the workers sick. Are you kidding me? These researchers dutifully took samples and they announced to the world, after a short pause, that they had found a unique virus. Wow. A virus that could kill millions of people around the world.

 

And the game was afoot. The lie that compounded into more lies.

 

CLEAN UP THE FECES! That should have been the “expert medical advice.” But of course it wasn’t, because who makes money from shoveling dung?

 

And then, several months later, the World Health Organization, BASED ON REPORTS OF 20, THAT’S 20 SO-CALLED CASES OF SWINE FLU, DECLARED THE “DISEASE” A LEVEL-SIX PANDEMIC…the highest threat level possible.

 

And in doing so, as documented by Peter Doshi in the British Medical Journal, the World Health Organization CHANGED ITS DEFINITION OF PANDEMIC SO THAT IT NO LONGER REQUIRED SEVERE WIDESPREAD DEATH.

 

They changed the definition.

 

But not the level of warning and concern and propaganda.

 

There is a lot more to this story, and I’ve written a number of articles about in this blog.

 

Point is, the official lies were taken apart one by one, and by the end, it was a debacle for the Church of Biological Mysticism. They retreated into the woodwork.

 

Understanding the nuts and bolts of propaganda and the subtleties, too, helps to take the machine apart and leave it on the ground, inoperative, next to the feces lagoons.

 

JON RAPPOPORT

 

Jon is the author of the new collection, THE MATRIX REVEALED, and, with Robert Scott Bell, a 10-hour audio seminar, VACCINES: ARMED AND DANGEROUS.

Jon Rappoport has worked as an investigative reporter for 30 years. Nominated for a Pulitzer Prize early in his career, Jon has published articles on medical fraud, and politics in LA Weekly, CBS Healthwatch, Spin, Stern, and other magazines and newspapers in the US and Europe.

www.nomorefakenews.com

qjrconsulting@gmail.com

ANATOMY OF A CONSPIRACY

ANATOMY OF A CONSPIRACY

MEDICAL MURDER IN THE MATRIX

MEDICALLY CAUSED DEATH IN AMERICA: AN EXCLUSIVE INTERVIEW WITH DR. BARBARA STARFIELD

by Jon Rappoport

March 8, 2012


Once in a while, I insert a plug for myself in an article. The purpose of this is to sell my products at www.nomorefakenews.com. Since the year 2001, I’ve probably written as many articles as anyone on the internet. They’re all free. So visit my store. Look over the seminars and consider buying one of them. Especially consider THE MATRIX REVEALED. End of plug.


I rerun this Dr. Barbara Starfield article — wherein I show you the email interview I did with Dr. Starfield in December 2009 — regarding her paper published in JAMA in July 2000 entitled Is US health really the best in the world?, just to push the wheel another turn.

The Starfield paper can be downloaded freely (as a .pdf) from here (via www.drug-education.info via en.wikipedia.org/wiki/Barbara_Starfield). The paper is fully cited as Starfield B. Is US health really the best in the world?. JAMA. 2000; 284(4):483-4. Dr. Barbara Starfield’s wiki page is here.

Each time I do this, I try to write a new introduction. Here is one…


The late Dr. Barbara Starfield exposed, in a prestigious mainstream medical journal, the horrific extent of medically caused death in America.

Since the July 26, 2000, publication of her review, “Is US health really the best in the world?”, there has been virtually no mainstream criticism of her findings.

And press coverage has been minimal. Articles did appear in 2000-2001, but then the issue itself vanished. So we have press silence, which is necessary and invaluable in any conspiracy.

We also have silence from the thousands of medical personnel who work as doctors, nurses, bureaucrats, teachers in medical schools, researchers and executives in pharmaceutical companies. And no one at the FDA has spoken up.

Well, this couldn’t be a conspiracy because too many people would have to be in on it.”

This is what we often hear when someone utters the word “conspiracy.” But you see, it happened here. And it happened here because, in part, the silent ones are trained not to question their education and the tons of propaganda issued by their bosses and by the so-called experts.

In other words, they are true believers. They aren’t attending meetings in rooms where they pledge secrecy and collaborate. They go along to get along. They keep their doubts to themselves to protect their jobs. They support the structure. They have faith in the efficacy and safety of modern medicine, because they been told what to think and what sources of evidence to accept.

If you put a black coat on a table and told them to look at it, they would say it was white.

At another level, we have the managers and supervisors and researchers and executives of drug companies. They know, of course, that any indictment of the safety of their drugs would threaten their jobs. They choose to believe their drugs are safe. They choose to believe all is well. They wear blinders. They trust the PR their own companies issue about the wonders of the drugs they sell.

And they are walled off from thinking about the dangers of drugs manufactured by other companies. They don’t look (or care to look) at the big picture.

Teachers in medical schools, which, like major media, are heavily financed by pharma money, ignore negative information about drugs. They pretend it doesn’t really exist. They pretend there are occasional scandals in an otherwise calm sea of progress and research.

At the drug companies, you of course have the outright liars and cheaters. They bury clinical trials of drugs that show the drugs are dangerous. They rationalize their actions in many ways. For example: “Well, you can always put together a study which will show a drug has negative effects. It happens. But if you do another study on the same drug, you could very well get a positive outcome. It’s unpredictable. We’re simply putting our best foot forward. The whole area of testing drugs on humans is fraught with with incontrollable variables…”

You add up all these factors and all these people working at different levels in the medical complex—including the doctors who write the prescriptions, who are trained to believe that any drug certified as safe by the FDA is really safe—and you have a de facto conspiracy.

And as Dr. Starfield pointed out in our interview, lobbyists in Washington and pharma money exert a powerful influence on elected and appointed government officials. Therefore, no Congressional investigations into drug safety and harm. No prosecutions. In fact, drug companies are now required to pay the FDA fees to finance that agency’s work in approving or denying approval to new drugs these companies want to market for public use. In other words, the drug companies are paying clients of the FDA.

That leaves only the question of intent. The intent to do harm.

A little common sense helps here. If I and other reporters can discover the true extent of the devastation caused by pharmaceutical drugs, then certainly highly placed medical bureaucrats and executives of drug companies are aware of the same data.

And among those people, and particularly among those who actually finance and own drug companies, there are individuals who consciously set out to achieve the results that are beyond debate: widespread debilitation, destruction, death. Or, alternatively, are quite willing to stand by and witness genocidal levels of “negligent homicide.”

Why do I say this? Because, to begin with, such people, knowing the overall effects of the drugs, are in a position to stop the carnage. But they don’t.


And then there is the circumstantial evidence of history. At the outbreak of World World 2, the most powerful pharmaceutical-chemical company in the world was IG Farben, the Nazi behemoth that actually put Hitler over the top in Germany and ensured he would be the dictator of the nation.

Farben established the pharmaceutical torture chamber along side the Auschwitz concentration camp, and paid to have prisoners brought to their lab for grotesque “medical experiments” on a regular basis.

Farben was composed of German companies, among which were Bayer, Hoescht, and BASF. At the close of the War, Farben executives were put on trial at Nuremberg. Among them, Fritz ter Meer, a high-ranking scientist-executive in Farben’s ranks.

Convicted of plunder and mass slavery, ter Meer was found guilty and sentenced to a mere seven years in prison. His sentence was commuted after four years. In 1954, he emerged as a member of the managing board of Bayer, which by then was running on high profits.

According to the Dr. Rath Foundation (which will offer immense amounts of information about Farben to the serious reader), ter Meer also became one of the architects of the Codex Alimentarius, that powerful organization dedicated to destroying the nutritional-supplement industry and the widespread benefits it provides.

I suggest several books: The Devil’s Chemists (Josiah E Du Bois); The Crime and Punishment of IG Farben (Joseph Borkin); Thy Will Be Done (Gerard Colby and Charlotte Dennett).

The last book is an immense exploration of Nelson Rockefeller’s quest to obtain and exploit natural resources in the South American Amazon region. This multi-faceted campaign, which involved a large missionary organization and several governments, resulted in the genocide of indigenous peoples.

Rockefeller-family interests of course include oil, pharmaceuticals, and the entire direction and paradigm of modern medical practice. The family’s Standard Oil company was a major partner with Farben for years.

Circumstantial evidence? Yes. But a great deal of future investigation is suggested here.


And now, reprinted, my interview with Dr. Barbara Starfield.

MEDICALLY CAUSED DEATH IN AMERICA

An Exclusive Interview With Dr. Barbara Starfield

by Jon Rappoport

The American health system, like clockwork, causes a mind-boggling number of deaths every year.

The figures have been known for a decade. The story was covered briefly when a landmark study surfaced, and then it sank like a stone.

The truth was inconvenient for many interests. That has not changed.

On July 26, 2000, the US medical community received a titanic shock to the system, when one of its most respected public-health experts, Dr. Barbara Starfield, revealed her findings on health care in America. Starfield was, and still is, associated with the Johns Hopkins School of Public Health. [Note: This interview was conducted in 2009. Dr. Starfield died in June, 2011.]

The Starfield study, “Is US health really the best in the world?”, published in the Journal of the American Medical Association, came to the following conclusions:

Every year in the US there are:

12,000 deaths from unnecessary surgeries;

7,000 deaths from medication errors in hospitals;

20,000 deaths from other errors in hospitals;

80,000 deaths from infections acquired in hospitals;

106,000 deaths from FDA-approved correctly prescribed medicines.

The total of medically-caused deaths in the US every year is 225,000.

This makes the medical system the third leading cause of death in the US, behind heart disease and cancer.

The Starfield study is the most disturbing revelation about modern health care in America ever published. The credentials of its author and the journal in which it appeared are, within the highest medical circles, impeccable.

On the heels of Starfield’s astonishing findings, media reporting was perfunctory, and it soon dwindled. No major newspaper or television network mounted an ongoing “Medicalgate” investigation. Neither the US Department of Justice nor federal health agencies undertook prolonged remedial action.

All in all, those parties who could have taken effective steps to correct this situation preferred to ignore it.


I interviewed Dr. Starfield by email (December 6-7, 2009). This is an edited version of the interview.

Q: In the medical research community, have your medically-caused mortality statistics been debated, or have these figures been accepted, albeit with some degree of shame?

A: The findings have been accepted by those who study them. There has been only one detractor, a former medical school dean, who has received a lot of attention for claiming that the US health system is the best there is and we need more of it. He has a vested interest in medical schools and teaching hospitals (they are his constituency).

Q: Have health agencies of the federal government consulted with you on ways to mitigate the effects of the US medical system?

A: NO.

Q: Are you aware of any systematic efforts, since your 2000 JAMA study was published, to remedy the main categories of medically caused deaths in the US?

A: No systematic efforts; however, there have been a lot of studies. Most of them indicate higher rates [of death] than I calculated.

Q: Can you offer an opinion about how the FDA can be so mortally wrong about so many drugs?

A: Yes, it cannot divest itself from vested interests. [There is] a large literature about this, mostly unrecognized by the people because the industry-supported media give it no attention.

Q: Did your 2000 JAMA study sail through peer review, or was there some opposition to publishing it?

A: It was rejected by the first journal that I sent it to, on the grounds that ‘it would not be interesting to readers’!

Q: Would it be correct to say that, when your JAMA study was published in 2000, it caused a momentary stir and was thereafter ignored by the medical community and by pharmaceutical companies?

A: Are you sure it was a momentary stir? I still get at least one email a day asking for a reprint—ten years later! The problem is that its message is obscured by those that do not want any change in the US health care system.

Q: Since the FDA approves every medical drug given to the American people, and certifies it as safe and effective, how can that agency remain calm about the fact that these medicines are causing 106,000 deaths per year?

A: Even though there will always be adverse events that cannot be anticipated, the fact is that more and more unsafe drugs are being approved for use. Many people attribute that to the fact that the pharmaceutical industry is (for the past ten years or so) required to pay the FDA for [product] reviews—which puts the FDA into an untenable position of working for the industry it is regulating. There is a large literature on this.

Q: Aren’t your 2000 findings a severe indictment of the FDA and its standard practices?

A: They are an indictment of the US health care industry: insurance companies, specialty and disease-oriented medical academia, the pharmaceutical and device manufacturing industries, all of which contribute heavily to re-election campaigns of members of Congress. The problem is that we do not have a government that is free of influence of vested interests. Alas, [it] is a general problem of our society—which clearly unbalances democracy.

Q: What was your personal reaction when you reached the conclusion that the US medical system was the third leading cause of death in the US?

A: I had previously done studies on international comparisons and knew that there were serious deficits in the US health care system, most notably in lack of universal coverage and a very poor primary care infrastructure. So I wasn’t surprised.

Q: Do the 106,000 deaths from medical drugs only involve drugs prescribed to patients in hospitals, or does this statistic also cover people prescribed drugs who are not in-patients in hospitals?

A: I tried to include everything in my estimates. Since the commentary was written, many more dangerous drugs have been added to the marketplace.


INTERVIEWER COMMENTS:

This interview with Dr. Starfield reveals that, even when an author has unassailable credentials within the medical-research establishment, the findings can result in no changes made to the system.

Yes, many persons and organizations within the medical system contribute to the annual death totals of patients, and media silence and public ignorance are certainly major factors, but the FDA is the assigned gatekeeper, when it comes to the safety of medical drugs. The buck stops there. If those drugs the FDA is certifying as safe are killing, like clockwork, 106,000 people a year, the Agency must be held accountable. The American people must understand that.

As for the other 119,000 people killed every year as a result of hospital treatment, this horror has to be laid at the doors of those institutions. Further, to the degree that hospitals are regulated and financed by state and federal governments, the relevant health agencies assume culpability.

It is astounding, as well, that the US Department of Justice has failed to weigh in on Starfield’s findings. If 225,000 medically caused deaths per year is not a crime by the Dept. of Justice’s standards, then what is?

To my knowledge, not one person in America has been fired from a job or even censured as result of these medically caused deaths.

The pharmaceutical giants stand back and carve up the populace into “promising markets.” They seek new disease labels and new profits from more and more toxic drugs. They do whatever they can—legally or illegally—to influence doctors in their prescribing habits. Some drug studies which cast new medicines in a negative light are buried. FDA panels are filled with doctors who have drug-company ties. Legislators are incessantly lobbied and supported with pharma campaign monies.

Nutrition, the cornerstone of good health, is ignored or devalued by most physicians. The FDA continues to attack nutritional supplements, even though the overall safety record of these nutrients is excellent, whereas, once again, the medical drugs the FDA certifies as safe are killing 106,000 Americans per year.

If you would care to add up the figures: FDA certified drugs are killing A MILLION people per decade.

No prosecutions? No federal remedy? No mainstream coverage of the biggest ongoing scandal in the nation?

Physicians are trained to pay exclusive homage to peer-reviewed published drug studies. These doctors unfailingly ignore the fact that, if medical drugs are killing a million Americans per decade, the studies on which those drugs are based must be fraudulent. In other words, the whole literature is suspect, unreliable, impenetrable, criminal.

© 2012 Jon Rappoport – All Rights Reserved

Jon is the author of the new collection, THE MATRIX REVEALED, and, with Robert Scott Bell, a 10-hour audio seminar, VACCINES: ARMED AND DANGEROUS.

Jon Rappoport has worked as an investigative reporter for 30 years. Nominated for a Pulitzer Prize early in his career, Jon has published articles on medical fraud, and politics in LA Weekly, CBS Healthwatch, Spin, Stern, and other magazines and newspapers in the US and Europe.

He is the is author of several books, including The Secret Behind Secret Societies and The Magic Agent (a novel).

Jon Rappoport

www.nomorefakenews.com

qjrconsulting@gmail.com

The Ethics of Killing Babies

by Jon Rappoport

March 6, 2012.

(To join our email list, click here.)

Buckle up.

A new article in the Journal of Medical Ethics proposes that newborn babies are not real persons, and therefore it is as ethical to kill them as it is to abort the unborn.

Here is the abstract of the article.

Abortion is largely accepted even for reasons that do not have anything to do with the fetus’ health. By showing that (1) both fetuses and newborns do not have the same moral status as actual persons, (2) the fact that both are potential persons is morally irrelevant and (3) adoption is not always in the best interest of actual people, the authors argue that what we call ‘after-birth abortion’ (killing a newborn) should be permissible in all the cases where abortion is, including cases where the newborn is not disabled.

(authors: Alberto Giubilini, Francesca Minerva; doi:10.1136/medethics-2011-100411)

(Ed. note: Here are more details about the article. The Journal of Medical Ethics shows the paper as “not found”.)

The authors argue that both fetuses and newborn babies lack the “moral status” of “actual persons.”

By this logic, many disabled people of adult age could be killed as well.

In fact, taking a person with a few problems and drugging him with antipsychotic medicines that routinely cause brain damage, you could create a human who no longer functions—and then you could kill him.

Moving on: the authors make the point that being “a potential person” is irrelevant. As long as the human can’t yet perceive goals and the notion of striving to achieve them, he is killable.

Point three: since abortion can be chosen for any reason, why not kill babies for any reason?

I’m trying to figure out why we should consider the authors of this paper fully formed human beings.

Do you ever get the feeling that ANY proposal, these days, is accorded merit and serious conversation re the pros and cons?

How about amputating the right arms of every person on Earth to bolster the obviously correct idea that we’re all fundamentally disabled?

Since pride goes before a fall, why not mutilate all persons and thereby eliminate the pride and the subsequent fall?

Why not extend the already broad class of victims by asserting that every parent without the freedom to kill his newborn baby is suffering from restrictive laws?

This month in Cincinnati, 30 teen mothers killed their babies. The city’s health department announced that figure is down 2% from last month…”


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Of course, the utterly insane proposal in this journal paper, if put into effect, would eventually cede to the State the absolute control of the process of infanticide. Because people at large are too crazy for that responsibility. Government, however, can make proper adjudications.

For example, in order to ensure funding for national health insurance is sufficient, the large sums spent on health care for the elderly can be cut by killing them en masse in their nursing homes. They had no goals left. No ambitions. They weren’t full persons.

I’m not warning you that these nightmares are coming to pass soon. But seeds are being planted.

And meanwhile, if you want to think about depopulation and radical disabling, you need look no further than mass vaccination of people with already-compromised immune systems, or immune systems not yet fully formed. Babies.

But the government and their medical allies say it’s okay. So it must be okay.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

The Liar’s Liar

The Liar’s Liar

Biggest Liar in America?

Who is Dr. Allen Frances?

by Jon Rappoport

February 27, 2012.

www.nomorefakenews.com

The medical cartel, one of a handful of evolving super-cartels that strive for more power every day, is rife with so much fraud it’s astounding. In the psychiatric arena, for example, an open secret has been bleeding out into public consciousness for the past ten years. I should know. I’m one of the people who has been exposing the secret:

THERE ARE NO DEFINITIVE PHYSICAL TESTS FOR ANY SO-CALLED MENTAL DISORDER.

And along with that:

ALL SO-CALLED MENTAL DISORDERS ARE ARBITRARILY INVENTED, NAMED, LABELED, DESCRIBED, AND CATEGORIZED by a committee of psychiatrists, from menus of human behaviors.

Their findings are published in periodically updated editions of The Diagnostic and Statistical Manual of Mental Disorders (DSM), printed by the American Psychiatric Association.

For years, even psychiatrists have been blowing the whistle on this hazy crazy process of “research.”

Of course, pharmaceutical companies, who manufacture highly toxic drugs to treat every one of these fictional disorders, are leading the charge to invent more and more mental-health categories, so they can sell more drugs and make more money.

But we have a mind-boggling twist. One of the great psychiatric honchos, who has been out in front inventing mental disorders, has gone public. He’s blown the whistle on himself and his colleagues.

His name is Dr. Allen Frances, and he made VERY interesting statements to Gary Greenberg, author of a Wired article: “Inside the Battle to Define Mental Illness,” (Dec.27, 2010).

I know. That’s a year and a half ago. But guess what? Major media never picked up on it in any serious way. It never became a scandal. It managed to fly below the radar.

Editors and reporters at major media outlets have an uncommon nose for avoiding the sort of trouble Greenberg’s piece would have created, were it to be unleashed on the population—and although they like to call themselves journalists, that’s a myth even they don’t really believe anymore. They’re mutts on short leashes.

Dr. Allen Frances is the man who, in 1994, headed up the project to write the latest edition of the psychiatric bible, the DSM-IV. This tome defines and labels and describes every official mental disorder in the known universe. The DSM-IV eventually listed 297 of them.

In an April 19, 1994, New York Times piece, “Scientist At Work,” Daniel Goleman called Frances “Perhaps the most powerful psychiatrist in America at the moment…”

Well, sure. If you’re sculpting the entire canon of diagnosable mental disorders for your colleagues, for insurers, for the government, for pharma (who will sell the drugs matched up to the 297 DSM-IV diagnoses), you’re right up there in the pantheon.

Long after the DSM-IV had been put into print, Dr. Frances talked to Wired’s Greenberg and said the following:

There is no definition of a mental disorder. It’s bullshit. I mean, you just can’t define it.”

BANG.

That’s on the order of the designer of the Hindenburg, looking at the burned rubble on the ground, remarking, “Well, I knew there would be a problem.”

After a suitable pause, Dr. Frances remarked to Greenberg, “These concepts [of distinct mental disorders] are virtually impossible to define precisely with bright lines at the borders.”

Obliquely, Frances might have been referring to the fact that his baby, the DSM-IV, had rearranged earlier definitions of ADHD and Bipolar to permit many MORE diagnoses, leading to a vast acceleration of drug-dosing with highly powerful and toxic compounds.

Finally, at the end of the Wired interview, Frances went off on a quite intriguing foray, advocating what amounts to a mass-population placebo effect which would justify the existence of the entire psychiatric profession.

Diagnosis [as spelled out in the DSM-IV] is part of the magic…you know those medieval maps? In the places where they didn’t know what was going on, they wrote ‘Dragons live here’…we have a dragon’s world here. But you wouldn’t want to be without the map.”

Here is the import of Dr. Frances’ words: People need to hope for the healing of their troubles; so even if we’re shooting blanks and pretending to know one kind of mental disorder from another, even if we’re inventing these mental-disorder definitions based on no biological or chemical diagnostic tests—since the tests don’t exist and we’re just juggling lists of behaviors—it’s a good thing, because people will then believe there is hope for them; they’ll believe it because we place a name on their problems…

If I were an editor at one of the big national newspapers, and one my reporters walked in and told me, “The most powerful psychiatrist in America just said the DSM is bullshit but it’s still important,” I think I’d make room on the front page.

If the reporter then added, “This shrink was in charge of creating the DSM-IV,” I’d clear more room above the fold.

If the reporter went on to explain that the whole profession of psychiatry would collapse overnight without the DSM, I’d call for a special section of the paper to be printed.

I’d tell the reporter to get ready to pound on this story day after day for months. I’d tell him to track down all the implications of Dr. Frances’ statements.

I’d open a bottle of champagne to toast the soon-to-be-soaring sales of my newspaper.

And then, of course, the next day I’d be fired.

Because there are powerful multi-billion-dollar interests at stake, and who in his right mind would challenge them?

And as I walked out of my job, I’d see a bevy of blank-eyed pharmaceutical executives marching into the office of the paper’s publisher, ready to read the riot act to him.

And as I chewed my cud and wandered the avenues of the big city, I’d look at all the people and something would seep in: the difference between the delusion called reality, which all these people accept, and the actual state of affairs: the giant con game, the giant shell game that allows the drugs to be sold, the drugs that—each and every one—deliver what the shrinks politely call “adverse effects.”

Look them up sometime, if you have a strong stomach.

Here is a sampling—and keep in mind that Dr. Frances’ work at the DSM IV allowed for MORE of these drugs to be prescribed, because the definition of Bipolar was expanded to include more people.


The Matrix Revealed


Adverse effects of Valproate (given for a Bipolar diagnosis) include:

acute, life-threatening, and even fatal liver toxicity;

life-threatening inflammation of the pancreas;

brain damage.

Adverse effects of Lithium (also given for a Bipolar diagnosis) include:

intercranial pressure leading to blindness;

peripheral circulatory collapse;

stupor and coma.

Adverse effects of Risperdal (given for “Bipolar” and “irritability stemming from autism”) include:

serious impairment of cognitive function;

fainting;

restless muscles in neck or face, tremors (may be indicative of motor brain damage).

Dr. Frances self-admitted label-juggling act also permitted the definition of ADHD to expand, thereby opening the door for greater and greater use of Ritalin as the treatment of choice.

So what about Ritalin?

In 1986, The International Journal of the Addictions published a most important literature review by Richard Scarnati. It was called “An Outline of Hazardous Side Effects of Ritalin (Methylphenidate)” [v.21(7), pp. 837-841].

Scarnati listed a large number of adverse affects of Ritalin and cited published journal articles which reported each of these symptoms.

For every one of the following (selected and quoted verbatim) Ritalin effects, there is at least one confirming source in the medical literature:

Paranoid delusions
Paranoid psychosis
Hypomanic and manic symptoms, amphetamine-like psychosis
Activation of psychotic symptoms
Toxic psychosis
Visual hallucinations
Auditory hallucinations
Can surpass LSD in producing bizarre experiences
Effects pathological thought processes
Extreme withdrawal
Terrified affect
Started screaming
Aggressiveness
Insomnia
Since Ritalin is considered an amphetamine-type drug, expect amphetamine-like effects
Psychic dependence
High-abuse potential DEA Schedule II Drug
Decreased REM sleep
When used with antidepressants one may see dangerous reactions including hypertension, seizures and hypothermia
Convulsions
Brain damage may be seen with amphetamine abuse.


power outside the matrix


A recent survey revealed that a high percentage of children diagnosed with bipolar had first received a diagnosis of ADHD. This is informative, because Ritalin and other speed-type drugs are given to kids who are slapped with the ADHD label. Speed, sooner or later, produces a crash. This is easy to call “clinical depression.” Then comes Prozac, Paxil, Zoloft. These drugs can produce temporary highs, followed by more crashes. The psychiatrist notices this up and down pattern—and then comes the diagnosis of Bipolar (manic-depression) and other drugs, including Valproate and Lithium.

In the US alone, there are at least 300,000 cases of motor brain damage incurred by people who have been prescribed so-called anti-psychotic drugs (aka “major tranquilizers”). Risperdal (mentioned above as a drug given to people diagnosed with Bipolar) is one of those major tranquilizers. (source: Toxic Psychiatry, Dr. Peter Breggin, St. Martin’s Press, 1991)

This psychiatric drug plague is accelerating across the land.

Where are the mainstream reporters and editors and newspapers and TV anchors who should be breaking this story and mercilessly hammering on it week after week? They are in harness.

And Dr. Frances is somehow let off the hook. He’s admitted in print that the whole basis of his profession is throwing darts at labels on a wall, and implies the “effort” is rather heroic—when, in fact, the effort leads to more and more poisonous drugs being dispensed to adults and children, to say nothing of the effect of being diagnosed with “a mental disorder.” I’m not talking about “the mental-disease stigma,” the removal of which is one of Hillary Clinton’s missions in life. No, I’m talking about MOVING A HUMAN INTO THE SYSTEM, the medical apparatus, where the essence of the game is trapping that person to harvest his money, his time, his energy, and of course his health—as one new diagnosis follows on another, and one new toxic treatment after another is undertaken, from cradle to grave. The result is a severely debilitated human being (if he survives), whose major claim to fame is his list of diseases and disorders, which he learns to wear like badges of honor.

Thank you, Dr. Frances.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at www.nomorefakenews.com

Part 2, Inventing Medical Reality

Part 2, Inventing Medical Reality

Placebo washout: Another outrageous medical coverup

by Jon Rappoport

February 24, 2012

NoMoreFakeNews.com

(Note: For part-1 of this article, click here.)

Here is yet another way to do medical studies that guarantee a waterfall of lies will spread out far and wide. Another way to make the studies look good when they aren’t.

Let’s say you went into a school to see if it was a good place for your child to acquire a real education. And you were shown overall performance records of the students on standardized tests, and these records looked quite impressive.

Upon inquiring a little further, though, you came across an interesting point. The head of the school believed that some students just didn’t perform well on tests—and so he had excused them from taking any exams.

Shocked, you said to him, “Your performance records are a sham. They don’t reflect the truth. You’ve stacked the deck.”

And he replied, “Not at all. I’ve merely kept statistics on those pupils who have the ability to take tests. That’s the important population. The others shouldn’t be tested at all. In this venue, they don’t count.”

Keep that analogy in mind as we proceed.

I want to alert you to a staggering medical practice in clinical trials of psychiatric drugs.

It’s called “placebo washout.”

Basically, it works this way. Before a drug company starts to test the effectiveness of a new medicine they want to market, they bring together all the volunteers—and they give them a sugar pill.

They tell them, “We’re going to give you a sugar pill.”

After a ten-day period on the placebo, the researchers weed out the people who improved, got better, feel better. They dump them from the ensuing clinical trial. Bye bye.

They don’t want these people around for the real clinical trial that is to follow.

Of course, they claim there are good reasons for this washout strategy. But the fact is, eliminating these volunteers from the study makes it far more likely that the drug being tested will look good, when it shouldn’t.

First, in case you don’t believe placebo washout is a real and widespread practice, here are two references that unequivocally state it is:

RP Greenberg et al, PMID 857037, PubMed-indexed for Medline;

and JG Rabkin et al, “Baseline Characteristics of 10-day placebo washout responders in antidepressant trials,” PMID.

It’s real. They give everybody a sugar pill, and then they dismiss all those who got better on it.

Then they get down to the actual clinical trial. They divide the remaining volunteers into two groups. Those who will receive the drug, and those who will be given another placebo.

Nobody is told which group they’re going to be in. That’s the whole point. Blinding the study enables researchers to compare the number of people who get better on the drug with those who get better on the placebo.

You see, it’s common knowledge that some people will get better on anything. That’s why they form the two groups. They have to prove (to the FDA) the drug is performing better than the sugar pill.

General estimates vary on what percentage of people get better on placebos. 35-45%, some researchers say, is a rule of thumb. Sometimes the % is higher.

But wait! The researchers ALREADY kicked out the people who got better on the sugar pill during the 10-day preliminary washout!

What’s going on here?

Well, in the actual clinical trial, where half the people get the placebo and half get the medicine, some people who get the placebo—armed with the hope that they might be getting the medicine—will feel better, even though they’re only swallowing sugar pills.

And the researchers must show that more people who are getting the drug are feeling better than those who are getting the placebo.

That’s the whole reason for this type of clinical trial.

See, 47 people who took the drug feel better. And only 22 people who took the sugar pill feel better. Therefore, the drug really works.”

Sure it works. Because you already kicked out all the people who felt better on a placebo in the washout phase.

In effect, you did a screening. You “cut out the competition.”

It’s like saying, “We have a great runner on our team. His times in the 100-meter dash are exceptional…there’s only one thing. In track meets, we insist he run only 80 meters and you have to imagine it’s 100.”

The FDA, which approves all drugs for public use, knows all about the placebo washout con job. Researchers know this. Shrinks know this. Drug companies know this. Even some medical reporters know this.

And yet, the practice goes on.

Placebo washout is on the order of saying, “Yes, we tested the new plane and it performs magnificently. Of course, we didn’t put it into the air. We rolled it across the runway.”

If there are any psychiatrists out there who are reading this, any researchers who want to defend placebo washout, I suggest we set up a debate with Dr. Peter Breggin, psychiatrist and author. But I warn you. Buckle up. It’ll be a bumpy ride.

Placebo washout. Rigging the game. Stacking the deck. The bigger the lie and the more obvious it is, the harder it is to believe that’s what’s you’re looking at. Until you LOOK.

In my 30 years as a reporter, I’ve come across maybe 100 scandals that could cause a significant sector of the medical cartel to burst into flames and blow away in the wind. This is one of those.

Of course, media, government, and drug corporations make sure such a thing never happens. And when I say media, I’m including publications you’d think would love to watch a really good fire. Turns out they have no stomach for it.

NOTE: In case you’re still a little shaky on this scam, let me lay it out this way:

A drug company has a new drug, Gx, for depression. It’s not on the market yet. For that they need FDA approval, and the approval rests on the results of a clinical trial the company is going to launch.

The company signs up 500 volunteers, all of whom meet mainstream criteria for a diagnosis of clinical depression.

The company brings together the 500 volunteers and administers them a sugar pill (placebo) for 10 days. Everybody knows it’s a sugar pill.

After 10 days, the company discovers which of the 500 people responded well to the pill: placebo effect. Let’s say 80 people did. They feel better. Boom. They’re dumped from further consideration. They’re gone.

Why? Because chances are very good that, were they allowed on to the next phase, those among them who ended up with the sugar pill would have said, “Wow, I feel better. I feel less depressed.”

And THAT means the people who were given the actual drug, Gx, would be “up against stiffer competition” from the group who took the placebo.

After those 80 people were booted from the placebo washout phase, with 420 volunteers left, they were divided into 2 groups of 210 each, and then 210 got the drug, Gx, and 210 got a sugar pill. None of the volunteers knows what they’re getting. This phase of the trial goes on for 6 weeks. At the end of that period, the study is “unblinded,” and everyone knows who got which pill. Now, among the placebo group of 210, it turns out that 60 showed significant improvement, and among the group of 210 who got Gx, 85 showed improvement.

The researchers conclude, “Those on Gx performed significantly better than those on placebo. This drug is good.”

But had those original 80, who were kicked to the side of the road after the placebo washout phase, been included in this later phase, the conclusions of the researchers could have turned out quite badly for the drug and the drug company. Gx could have performed no better than the sugar pill. It could have done worse.

And this is called SCIENCE.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com.

Inventing Medical Reality

Inventing Medical Reality

by Jon Rappoport

February 20, 2012

NoMoreFakeNews.com

(Note: For part-2 of this article, click here.)

“It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” —Marcia Angell, MD

The secret of acting is sincerity. If you can fake that, you’ve got it made.” —George Burns

I’ve been asked to reprint this piece. And in light of my recent release of THE MATRIX REVEALED, the information in this piece takes on special meaning. The faking of medical reality is, at bottom, an operation designed to bolster the power of the medical cartel, one of the most important forces on the planet.

What do doctors rely on? What do medical schools rely on? What do medical journals and mainstream medical reporters and drug companies and the FDA rely on?

The sanctity of published clinical trials of drugs. These trials determine whether the drugs are safe and effective. The drugs are tested on human volunteers. The results are tabulated. The trial is described in a paper that is printed by a medical journal.

This is science. This is rationality. This is the rock. Without these studies, the whole field of medical research would fall apart in utter chaos.

Upon this rock, and hence through media, the public becomes aware of the latest breakthrough, the newest medicine. Through doctors in their offices, the public finds out what drugs they should take—and their doctors know because their doctors have read the published reports in the medical journals, the reports that describe the clinical trials. Or if the doctors haven’t actually read the reports, they’ve been told about them.

It all goes back to this rock.

And when mainstream advocates attack so-called alternative or natural health, they tend to mention that their own sacred profession is based on real science, on studies, on clinical trials.

One doctor told me, “The clinical trials and published studies are what keep us from going back to the Stone Age.”

So now let me quote a recent article in the NY Review of Books (May 12, 2011) by Helen Epstein, “Flu Warning: Beware the Drug Companies.”

Six years ago, John Ioannidis, a professor of epidemiology at the University of Ioannina School of Medicine in Greece, found that nearly half of published articles in scientific journals contained findings that were false, in the sense that independent researchers couldn’t replicate them. The problem is particularly widespread in medical research, where peer-reviewed articles in medical journals can be crucial in influencing multimillion- and sometimes multibillion-dollar spending decisions. It would be surprising if conflicts of interest did not sometimes compromise editorial neutrality, and in the case of medical research, the sources of bias are obvious. Most medical journals receive half or more of their income from pharmaceutical company advertising and reprint orders, and dozens of others [journals] are owned by companies like Wolters Kluwer, a medical publisher that also provides marketing services to the pharmaceutical industry.”

Here’s another quote from the same article:

The FDA also relies increasingly upon fees and other payments from the pharmaceutical companies whose products the agency is supposed to regulate. This could contribute to the growing number of scandals in which the dangers of widely prescribed drugs have been discovered too late. Last year, GlaxoSmithKline’s diabetes drug Avandia was linked to thousands of heart attacks, and earlier in the decade, the company’s antidepressant Paxil was discovered to exacerbate the risk of suicide in young people. Merck’s painkiller Vioxx was also linked to thousands of heart disease deaths. In each case, the scientific literature gave little hint of these dangers. The companies have agreed to pay settlements in class action lawsuits amounting to far less than the profits the drugs earned on the market. These precedents could be creating incentives for reduced vigilance concerning the side effects of prescription drugs in general.”

Also from the NY Review of Books, here are two quotes from Marcia Angell, former editor-in-chief of The New England Journal of Medicine, perhaps the most prestigious medical journal in the world. (“Drug Companies and Doctors: A Story of Corruption”)

Consider the clinical trials by which drugs are tested in human subjects. Before a new drug can enter the market, its manufacturer must sponsor clinical trials to show the Food and Drug Administration that the drug is safe and effective, usually as compared with a placebo or dummy pill. The results of all the trials (there may be many) are submitted to the FDA, and if one or two trials are positive—that is, they show effectiveness without serious risk—the drug is usually approved, even if all the other trials are negative.”

Here is another Angell statement:

In view of this control and the conflicts of interest that permeate the enterprise, it is not surprising that [drug] industry-sponsored trials published in medical journals consistently favor sponsors’ drugs—largely because negative results are not published, positive results are repeated in slightly different forms, and a positive spin is put on even negative results. A review of seventy-four clinical trials of antidepressants, for example, found that thirty-seven of thirty-eight positive studies were published. But of the thirty-six negative studies, thirty-three were either not published or published in a form that conveyed a positive outcome.”

It turns out that the source of the informational pipeline that feeds the entire perception of pharmaceutical medicine is a rank fraud.

It would be on the order of an intelligence agency discovering that the majority of its operatives were actually working for the other side.

And then continuing on with business as usual.

Sometimes the body is dead even though it keeps on walking. It can smile and nod and perform basic functions—a zombie—but it is doing so only because certain implacable criminals back it up and give it a machine-like force.

We have the clinical trials of studies on drugs and they are published in top-rank journals. We are the epitome of science.”

Yes, false science. Riddled from top to bottom with lies.

Perhaps this will help the next time a friend, pretending he actually knows anything, tells you pharmaceutical medicine is a resounding success.

If you need more, cite Dr. Barbara Starfield’s famous study, “Is US health really the best in the world?” Journal of the American Medical Association, July 26, 2000. Starfield concludes that 225,000 people are killed by the medical system in the US every year—106,000 by FDA-approved medicines. That latter figure would work out to over a MILLION deaths per decade.

A final note: The august editors of medical journals have a game they can play. Suppose a drug company has just finished writing up the results of a clinical drug trial and has submitted the piece to a journal for publication. The editor knows the company carried out a half-dozen other such trials on the same drug…and they didn’t look good. The drug caused wild fluctuations in blood pressure and blood sugar. There were heart attacks. Strokes. But this ONE study, the one submitted for publication, looks very positive. The editor knows if he prints it and forgets about “ethics,” the drug company will order re-prints of the piece from him and distribute them to doctors all over the world, and to reporters, professors, government officials. The drug company will order and pay for so many re-prints, the medical journal can make $700,000 from publishing THAT ONE STUDY. Let’s see. In one hand, the editor sees: I won’t publish it=no money. In the other hand, he sees: I’ll publish it=$700,000. What to do?

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com.

The school shooting white paper

Why did they do it?

An inquiry into the school shootings in America (1999)

by Jon Rappoport

February 11, 2012

(To join our email list, click here.)

(Published (1999) by the Truth Seeker Foundation.)

The massacre at Columbine High School took place on April 20, 1999. Astonishingly, for eight days after the tragedy, during thousands of hours of prime-time television coverage, virtually no one mentioned the word “drugs.” Then the issue was opened. Eric Harris, one of the shooters at Columbine, was on at least one drug.

The NY Times of April 29, 1999, and other papers reported that Harris was rejected from enlisting in the Marines for medical reasons. A friend of the family told the Times that Harris was being treated by a psychiatrist. And then several sources told the Washington Post that the drug prescribed as treatment was Luvox, manufactured by Solvay.

In two more days, the “drug-issue” was gone.

Luvox is of the same class as Prozac and Zoloft and Paxil. They are labeled SSRIs (selective serotonin reuptake inhibitors). They attempt to alleviate depression by changing brain-levels of the natural substance serotonin. Luvox has a slightly different chemical configuration from Prozac, Paxil, and Zoloft, and it was approved by the FDA for obsessive-compulsive disorder, although many doctors apparently prescribe it for depression.

Had Eric Harris been on other drugs as well? Ritalin? Prozac? Tranquilizers? As yet we don’t know.

Prozac is the wildly popular Eli Lilly antidepressant which has been linked to suicidal and homicidal actions. It is now given to young children. Again, its chemical composition is very close to Luvox, the drug that Harris took.

Dr. Peter Breggin, the eminent psychiatrist and author (Toxic Psychiatry, Talking Back to Prozac, Talking Back to Ritalin), told me, “With Luvox there is some evidence of a four-percent rate for mania in adolescents. Mania, for certain individuals, could be a component in grandiose plans to destroy large numbers of other people. Mania can go over the hill to psychosis.”

Dr. Joseph Tarantolo is a psychiatrist in private practice in Washington DC. He is the president of the Washington chapter of the American Society of Psychoanalytic Physicians. Tarantolo states that “all the SSRIs [including Prozac and Luvox] relieve the patient of feeling. He becomes less empathic, as in `I don’t care as much,’ which means `It’s easier for me to harm you.’ If a doctor treats someone who needs a great deal of strength just to think straight, and gives him one of these drugs, that could push him over the edge into violent behavior.”

In Arianna Huffington’s syndicated newspaper column of July 9, 1998, Dr. Breggin states, “I have no doubt that Prozac can cause or contribute to violence and suicide. I’ve seen many cases. In a recent clinical trial, 6 percent of the children became psychotic on Prozac. And manic psychosis can lead to violence.”

Huffington follows up on this: “In addition to the case of Kip Kinkel, who had been a user of Prozac [Kinkel was the shooter in the May 21, 1998, Springfield, Oregon, school massacre], there are much less publicized instances where teenagers on Prozac or similar antidepressants have exploded into murderous rages: teenagers like Julie Marie Meade from Maryland who was shot to death by the police when they found her waving a gun at them. Or Ben Garris, a 16-year old in Baltimore who stabbed his counselor to death. Or Kristina Fetters, a 14-year old from Des Moines, Iowa, who stabbed her favorite great aunt in a rage that landed her a life sentence.”

Dr. Tarantolo also has written about Julie Marie Meade. In a column for the ICSPP (International Center for the Study of Psychiatry and Psychology) News, “Children and Prozac: First Do No Harm,” Tarantolo describes how Julie Meade, in November of 1996, called 911, “begging the cops to come and shoot her. And if they didn’t do it quickly, she would do it to herself. There was also the threat that

she would shoot them as well.”

The police came within a few minutes, “5 of them to be exact, pumping at least 10 bullets into her head and torso.”

Tarantolo remarks that a friend of Julie said Julie “had plans to make the honor roll and go to college. He [the friend] had also observed her taking all those pills.” What pills? Tarantolo called the Baltimore medical examiner, and spoke with Dr. Martin Bullock, who was on a fellowship at that office. Bullock said, “She had been taking Prozac for four years.”

Tarantolo asked Bullock, “Did you know that Prozac has been implicated in impulsive de novo violence and suicidalness?” Bullock said he was not aware of this.

Tarantolo writes, “Had she recently increased the dosage? Was she taking other drugs? Drugs such as Ritalin, cocaine, amphetamine, and tricyclic antidepressants (Tofranil, Pamelor, Elavil) could all potentiate the effect of the SSRI (selective serotonin reuptake inhibitors include Prozac, Zoloft and Paxil).”

In layman’s language, mixing these drugs could tinker in ignorance with basic brain chemistry and bring on horrendous violent behavior.

Tarantolo is careful to point out, “A change [in Julie’s drug-taking pattern] was not necessary, though, to explain her behavior. Violent and suicidal behavior have been observed both early (a few weeks) and late (many months) in treatment with Prozac.”

The November 23rd, 1996, Washington Post reported the Julie Meade death by shooting. The paper mentioned nothing about Prozac. This was left to a more penetrating newspaper, the local PG County Journal-the Maryland county in which the shooting took place.

Why did the Post never mention Prozac or interview any of a growing number of psychiatrists who have realized the danger of giving these drugs to children (and adults)?

Is it because major media outlets enjoy considerable support from pharmaceutical advertisers? Is it because these companies have been running successful PR campaigns to keep their drugs’ names quiet when suicides and murders are reported?

Another small paper, The Vigo Examiner (Terra Haute, Indiana), looked into the May 21, 1998, murders in Springfield, Oregon. The shooter, who had been on Prozac, Kip Kinkel, was a 15-year-old freshman. First he killed his parents, then walked into his school cafeteria and gunned down fellow students. He killed 2 and wounded 22. He is awaiting trial.

Vigo Examiner reporter Maureen Sielaff covered this story. Showing straightforward independence where many big-time reporters just don’t, Sielaff researched the book, Prozac and Other Psychiatric Drugs, by Lewis A. Opler, MD. She writes, “The following side effects are listed for Prozac: apathy; hallucinations; hostility; irrational ideas; paranoid reactions; antisocial behavior; hysteria; and suicidal thoughts.” An explosive cocktail of symptoms.

A day or two after the Littleton, Colorado, shootings, a teenager in Los Angeles, depressed about Littleton, hung himself. The boy had been under treatment for depression. Did that mean Prozac? Zoloft? Luvox? Will any reporter look into that incident?

The Jonesboro, Arkansas, school shooting took place on March 24, 1998. Mitchell Johnson, 13, and Andrew Golden, 11, apparently faked a fire alarm at Westside Middle School. Then when everyone came outside, the boys fired from the nearby woods, killing four students and a teacher, wounding 11 other people. Charged as juveniles, the boys were convicted of capital murder and battery. They can be held in jail until they are 21 years old. Dr. Alan Lipman, of Georgetown University, one of the experts interviewed on network television after Littleton, remarked that at least one of the boys who committed murder in Jonesboro had been, before the incident, treated for violent behavior. Treated how? With Prozac, with Zoloft, with a combination of antidepressants? The action of these drugs-altering the supply of the brain neurotransmitter serotonin-is touted by some people as a potential cure for violence. The only problem is, there is no acknowledged proof within the broad psychiatric profession that serotonin is a causative factor in violence. That is an unproven theory.

Not that unproven theories stop the dedicated from experimenting on brains of the young.

We must get a complete review of the medical history of the two Littleton shooters, Eric Harris and Dylan Klebold.

In the aftermath of other school shootings, have parents tried to find answers? With what responses have their efforts been met?

In Olivehurst, California, on May 1, 1992, Eric Houston, 20, killed 4 people and wounded 10 at his former high school. Houston was sentenced to death.

On January 18, 1993, in Grayhurst, Kentucky, Scott Pennington, 17, entered Deanna McDavid’s English class at East Carter High School and shot her in the head. He also shot Marvin Hicks, the school janitor, in the stomach. Pennington was sentenced to life, without the possibility of parole for 25 years.

In Richmond, Virginia, on October 30, 1995, Edward Earl Spellman, 18, shot and wounded 4 students outside their high school.

On February 2, 1996, in an algebra class at Frontier Junior High School in Mose Lake, Washington, Barry Loukaitas, 14, killed his teacher and 2 teen-aged boys with an assault rifle, and wounded a girl. Loukaitas was sentenced to 2 mandatory life terms.

In St. Louis, Missouri, on February 29, 1996, Mark Boyd, 30, fired into a school bus when its doors opened, killed a 15-year-old pregnant girl and wounded the driver.

On July 26, 1996, Yohao Albert, a high-school junior, shot and wounded 2 classmates in a stairwell at his Los Angeles school.

On February 19, 1997, in Bethel, Alaska, Evan Ramsey, 16, shot and killed his high school principal Ron Edwards and one of his classmates, Josh Palacious. Two students were wounded. Ramsey was sentenced to 2 99-year terms. Authorities later accused 2 students of knowing the shootings were

going to happen.

On October 1, 1997, in Pearl, Mississippi, Luke Woodham, 16, started shooting in his school cafeteria. He killed 2 students, including his ex-girlfriend, and wounded 7 others. He also killed his mother. Woodham was sentenced to life. Authorities later accused 6 friends of conspiracy.

On December 1, 1997, at Heath High School in West Paducah, Kentucky, Michael Carneal, 14, found students coming out of a prayer meeting. Using a stolen pistol, he shot 8 of these students and killed 3. One of the wounded girls is paralyzed.

On December 15, 1997, in Stamps, Arkansas, Joseph Todd, 14, was arrested in the shooting of 2 students outside their high school. The students recovered from their wounds. Todd faces trial.

In Edinboro, Pennsylvania, on April 24, 1998, Andrew Wurst, 14, allegedly shot and killed his science teacher, John Gillette, at the JW Parker Middle School at an 8th grade dance. Two students and another teacher were wounded. Wurst is awaiting trial.

In Fayetteville, Tennessee, on May 19, 1998, several days before graduation, Jacob Davis, 18, allegedly shot and killed Robert Creson, a classmate at Lincoln County High School. Creson was dating Davis’ ex-girlfriend. Davis, who was an honor student, awaits trial.

Try to find major media coverage of these crimes that carefully examines the medical-drug history of the perpetrators and establishes whether or not they were on drugs that could significantly contribute to violence.

A CNN story, dated May 21, 1998, authored by its Justice Dept. correspondent, Pierre Thomas, offered the following statistics: “Ten percent of the nation’s schools reported one or more violent crimes in the 1996-1997 school year, including murder, suicide, rape, robbery and fights involving weapons.” Even if these Justice Dept. figures are self-serving and overblown, they point to a chilling landscape.

The availability (to children) of guns is a cause. No question.

The saturation of violence on TV is a cause. No question.

The breakup of families is a cause. No question. So is outright child abuse.

The compartmentalization of children from their parents is a cause.

The absence of a good education is a cause.

The growing poverty and its atmosphere of hopelessness in America is a cause.

The presence of lunatic ideologies (Nazism, Satanism) in the landscape is a factor.

You can’t assign numbers to these causes. You can’t say one of the above is a 23% cause or a 3% cause.

But is there another factor in pushing kids over the edge? Are some children, angry and desperate and in proximity to weapons, who are nevertheless quite able to maintain moral equilibrium, being jolted by chemicals which are scrambling their brains and intensifying their impulses and amplifying their dark thoughts?

The bulk of American media appears afraid to go after psychiatric drugs as a cause. This fear stems, in part, from the sure knowledge that expert attack dogs are waiting in the wings, funded by big-time pharmaceutical companies. There are doctors and researchers as well who have seen a dark truth about these drugs in the journals, but are afraid to stand up and speak out. After all, the medical culture punishes no one as severely as its own defectors, when defection from the party line threatens profits and careers and reputations, when defection alerts the public that deadly effects could be emanating from corporate boardrooms.

And what of the federal government itself? The FDA licenses every drug released for public use and certifies that it is safe and effective. If a real tornado started at the public level, if the mothers of the young killers and young victims began to see a terrible knowledge swim into view, a knowledge they hadn’t imagined, and if THEY joined forces, the earth would shake.

After commenting on some of the adverse effects of the antidepressant drug Prozac, psychiatrist Peter Breggin notes, “From the initial studies, it was also apparent that a small percentage of Prozac patients became psychotic.”

Prozac, in fact, endured a rocky road in the press for a time. Stories on it rarely appear now. The major media have backed off. But on February 7th, 1991, Amy Marcus’ Wall Street Journal article on the drug carried the headline, “Murder Trials Introduce Prozac Defense.” She wrote, “A spate of murder trials in which defendants claim they became violent when they took the antidepressant Prozac are imposing new problems for the drug’s maker, Eli Lilly and Co.”

Also on February 7, 1991, the New York Times ran a Prozac piece headlined, “Suicidal Behavior Tied Again to Drug: Does Antidepressant Prompt Violence?”

In his landmark book, Toxic Psychiatry, Dr. Breggin mentions that the Donahue show (Feb. 28, 1991) “put together a group of individuals who had become compulsively self-destructive and murderous after taking Prozac and the clamorous telephone and audience response confirmed the problem.”

Breggin also cites a troubling study from the February 1990 American Journal of Psychiatry (Teicher et al, v.147:207-210) which reports on “six depressed patients, previously free of recent suicidal ideation, who developed `intense, violent suicidal preoccupations after 2-7 weeks of fluoxetine [Prozac] treatment.’ The suicidal preoccupations lasted from three days to three months after termination of the treatment. The report estimates that 3.5 percent of Prozac users were at risk. While denying the validity of the study, Dista Products, a division of Eli Lilly, put out a brochure for doctors dated August 31, 1990, stating that it was adding `suicidal ideation’ to the adverse events section of its Prozac product information.”

An earlier study, from the September 1989 Journal of Clinical Psychiatry, by Joseph Lipiniski, Jr., indicates that in five examined cases people on Prozac developed what is called akathesia. Symptoms include intense anxiety, inability to sleep, the “jerking of extremities,” and “bicycling in bed or just turning around and around.” Breggin comments that akathesia “may also contribute to the drug’s tendency to cause self-destructive or violent tendencies … Akathesia can become the equivalent of biochemical torture and could possibly tip someone over the edge into self-destructive or violent behavior … The June 1990 Health Newsletter, produced by the Public Citizen Research Group, reports, ‘Akathesia, or symptoms of restlessness, constant pacing, and purposeless movements of the feet and legs, may occur in 10-25 percent of patients on Prozac.'”

The well-known publication, California Lawyer, in a December 1998 article called “Protecting Prozac,” details some of the suspect maneuvers of Eli Lilly in its handling of suits against Prozac. California Lawyer also mentions other highly qualified critics of the drug: “David Healy, MD, an internationally renowned psychopharmacologist, has stated in sworn deposition that `contrary to Lilly’s view, there is a plausible cause-and-effect relationship between Prozac’ and suicidal-homicidal events. An epidemiological study published in 1995 by the British Medical Journal also links Prozac to increased suicide risk.”

When pressed, proponents of these SSRI drugs sometimes say, “Well, the benefits for the general population far outweigh the risk,” or, “Maybe in one or two tragic cases the dosage prescribed was too high.” But the problem will not go away on that basis. A shocking review-study published in The Journal of Nervous and Mental Diseases (1996, v.184, no.2), written by Rhoda L. Fisher and Seymour Fisher, called “Antidepressants for Children,” concludes: “Despite unanimous literature of double-blind studies indicating that antidepressants are no more effective than placebos in treating depression in children and adolescents, such medications continue to be in wide use.”

In wide use. This despite such contrary information and the negative, dangerous effects of these drugs.

There are other studies: “Emergence of self-destructive phenomena in children and adolescents during fluoxetine treatment,” published in the Journal of the American Academy of Child and Adolescent Psychiatry (1991, vol.30), written by RA King, RA Riddle, et al. It reports self-destructive phenomena in 14% (6/42) of children and adolescents (10-17 years old) who had treatment with fluoxetine (Prozac) for obsessive-compulsive disorder.

July, 1991. Journal of Child and Adolescent Psychiatry. Hisako Koizumi, MD, describes a thirteen-year-old boy who was on Prozac: “full of energy,” “hyperactive,” “clown-like.” All this devolved into sudden violent actions which were “totally unlike him.”

September, 1991. The Journal of the American Academy of Child and Adolescent Psychiatry. Author Laurence Jerome reports the case of a ten-year old who moves with his family to a new location. Becoming depressed, the boy is put on Prozac by a doctor. The boy is then “hyperactive, agitated … irritable.” He makes a “somewhat grandiose assessment of his own abilities.” Then he calls a stranger on the phone and says he is going to kill him. The Prozac is stopped, and the symptoms disappear.

Recently I spoke with a psychologist at a major university about the possibility that Prozac could have provoked some of the school shootings. He said, “Well, in the case of Columbine High School, that couldn’t have been the case. The boy had a whole plan there. Prozac is more of an impulse-causer.” I said, “Suppose the plan was in the realm of a maybe-fantasy and then Prozac pushed the whole thing over the edge.” After a pause he said, “Yes, that could be.” As mentioned above, grandiose ideas can be generated by a person taking Prozac, and in the literature there is also mention of a “delusional system” being the outcome in a case of a patient on the drug.

A December 1, 1996, newswire story from Cox News Service, by Gary Kane, states, “Scores of young men and women across the country are learning that the Ritalin they took as teen-agers is stopping them from serving their country or starting a military career.”

Kane continues, “All branches of the armed forces reject potential enlistees who use Ritalin or similar behavior-modifying medications … And people who took Ritalin as teen-agers to treat ADD [Attention Deficit Disorder], an inhibitor of academic skills, are rejected from military service, even if they no longer take the medication.”

Was this the case with Eric Harris? Was he rejected by the Marines only because of the Luvox, or was Ritalin use, past or present, involved as well?

Ritalin, manufactured by Novartis, is the close cousin to speed which is given to perhaps two million American schoolchildren for a condition called Attention Deficit Disorder (ADD), or ADHD (Attention Deficit Hyperactivity Disorder). ADD and ADHD, for which no organic causes have ever been found, are touted as disease-conditions that afflict the young, causing hyperactivity, unmanageability, and learning problems. Of course, when you name a disorder or a syndrome and yet can find no single provable organic cause for it, you have nothing more than a loose collection of behaviors with an arbitrary title.

Correction: you also have a pharmaceutical bonanza.

Dr. Breggin, referring to an official directory of psychiatric disorders, the DSM-III-R, writes that withdrawal from amphetamine-type drugs, including Ritalin, can cause “depression, anxiety, and irritability as well as sleep problems, fatigue, and agitation.” Breggin then remarks, “The individual may become suicidal in response to the depression.”

The well-known Goodman and Gilman’s The Pharmacological Basis of Therapeutics reveals a strange fact. It states that Ritalin is “structurally related to amphetamines … Its pharmacological properties are essentially the same as those of the amphetamines.” In other words, the only clear difference is legality. And the effects, in layman’s terms, are obvious. You take speed and after awhile, sooner or later, you start crashing. You become agitated, irritable, paranoid, delusional, aggressive.

A firm and objective medical review needs to be done in all of the school shootings, to determine how many of the shooters were on, or had at one time been on, Ritalin.

In Toxic Psychiatry, Dr. Breggin discusses the subject of drug combinations: “Combining antidepressants [e.g., Prozac, Luvox] and psychostimulants [e.g., Ritalin] increases the risk of cardiovascular catastrophe, seizures, sedation, euphoria, and psychosis. Withdrawal from the combination can cause a severe reaction that includes confusion, emotional instability, agitation, and aggression.” Children are frequently medicated with this combination, and when we highlight such effects as aggression, psychosis, and emotional instability, it is obvious that the result is pointing toward the very real possibility of violence.

In 1986, The International Journal of the Addictions published a most important literature review by Richard Scarnati. It was called “An Outline of Hazardous Side Effects of Ritalin (Methylphenidate”) [v.21(7), pp. 837-841].

Scarnati listed over a hundred adverse affects of Ritalin and indexed published journal articles for each of these symptoms.

For every one of the following (selected and quoted verbatim) Ritalin effects then, there is at least one confirming source in the medical literature:

• Paranoid delusions

• Paranoid psychosis

• Hypomanic and manic symptoms, amphetamine-like psychosis

• Activation of psychotic symptoms

• Toxic psychosis

• Visual hallucinations

• Auditory hallucinations

• Can surpass LSD in producing bizarre experiences

• Effects pathological thought processes

• Extreme withdrawal

• Terrified affect

• Started screaming

• Aggressiveness

• Insomnia

• Since Ritalin is considered an amphetamine-type drug, expect amphatamine-like effects

• psychic dependence

• High-abuse potential DEA Schedule II Drug

• Decreased REM sleep

• When used with antidepressants one may see dangerous reactions including hypertension, seizures and hypothermia

• Convulsions

• Brain damage may be seen with amphetamine abuse.

Many parents around the country have discovered that Ritalin has become a condition for their children continuing in school. There are even reports, by parents, of threats from social agencies: “If you don’t allow us to prescribe Ritalin for your ADD child, we may decide that you are an unfit parent. We may decide to take your child away.”

This mind-boggling state of affairs is fueled by teachers, principals, and school counselors, none of whom have medical training.

Yet the very definition of the “illnesses” for which Ritalin would be prescribed is in doubt, especially at the highest levels of the medical profession. This doubt, however, has not filtered down to most public schools.

In commenting on Dr. Lawrence Diller’s book, Running on Ritalin, Dr. William Carey, Director of Behavioral Pediatrics, Children’s Hospital of Philadelphia, has written, “Dr. Diller has correctly described … the disturbing trend of blaming children’s social, behavioral, and academic performance problems entirely on an unproven brain deficit…”

On November 16-18, 1998, the National Institute of Mental Health held the prestigious “NIH Consensus Development Conference on Diagnosis and Treatment of Attention Deficit Hyperactivity Disorder [ADHD].” The conference was explicitly aimed at ending all debate about the diagnoses of ADD, ADHD, and about the prescription of Ritalin. It was hoped that at the highest levels of medical research and bureaucracy, a clear position would be taken: this is what ADHD is, this is where it comes from, and these are the drugs it should be treated with. That didn’t happen, amazingly. Instead, the official panel responsible for drawing conclusions from the conference threw cold water on the whole attempt to reach a comfortable consensus.

Panel member Mark Vonnegut, a Massachusetts pediatrician, said, “The diagnosis [of ADHD] is a mess.”

The panel essentially said it was not sure ADHD was even a “valid” diagnosis. In other words, ADD and ADHD might be nothing more than attempts to categorize certain children’s behaviors-with no organic cause, no clear-cut biological basis, no provable reason for even using the ADD or ADHD labels.

The panel found “no data to indicate that ADHD is due to a brain malfunction [which malfunction had been the whole psychiatric assumption].”

The panel found that Ritalin has not been shown to have long-term benefits. In fact, the panel stated that Ritalin has resulted in “little improvement on academic achievement or social skills.”

Panel chairman, David Kupfer, professor of psychiatry at the University of Pittsburgh, said, “There is no current validated diagnostic test [for ADHD].”

Yet at every level of public education in America, there remains what can only be called a voracious desire to give children Ritalin (or other similar drugs) for ADD or ADHD.

Nullifying the warnings, assurances and prescriptions doctors routinely give to parents of children who have been diagnosed ADD or ADHD should be a national goal.

The following pronouncement makes a number of things clear: The 1994 Textbook of Psychiatry, published by the American Psychiatric Press, contains this review (Popper and Steingard)-“Stimulants [such as Ritalin] do not produce lasting improvements in aggressivity, conduct disorder, criminality, education achievement, job functioning, marital relationships, or long-term adjustment.”

Parents should also wake up to the fact that, in the aftermath of the Littleton, Colorado, tragedy, pundits and doctors are urging more extensive “mental health” services for children. Fine, except whether you have noticed it or not, this no longer means, for the most part, therapy with a caring professional. It means drugs. It means the drugs I am discussing in this inquiry.

In December 1996, the US Drug Enforcement Agency held a conference on ADHD and Ritalin. Surprisingly, it issued a sensible statement about drugs being a bad substitute for the presence of caring parents: “[T]he use of stimulants [such as Ritalin] for the short-term improvement of behavior and underachievement may be thwarting efforts to address the children’s real issues, both on an individual and societal level. The lack of long-term positive results with the use of stimulants and the specter of previous and potential stimulant abuse epidemics, give cause to worry about the future. The dramatic increase in the use of methylphenidate [Ritalin] in the 1990s should be viewed as a marker or warning to society about the problems children are having and how we view and address them.”

The Brookhaven National Laboratory has studied Ritalin through PET scans. Lab researchers have found that the drug decreased the flow of blood to all parts of the brain by 20-30%.

That is of course a very negative finding. It is a signal of danger.

But parents, teachers, counselors, principals, school psychologists know nothing about this. Nor do they know that cocaine produces the same blood-flow effect.

In his book, Talking Back to Ritalin, Peter Breggin expands on the drug’s effects: “Stimulants such as Ritalin and amphetamine … have grossly harmful impacts on the brain-reducing overall blood flow, disturbing glucose metabolism, and possibly causing permanent shrinkage or atrophy of the brain.”

In the wake of the Littleton shooting, we find that “the American people” and lawyers and pundits and child psychologists are pointing the finger at Hollywood, at video games like Doom, at inattentive parents, and at the availability of guns. We have to wonder why almost no one is calling out these drugs.

Is it possible that the work of PR people is shaping the national response?

An instructive article, “Protecting Prozac,” by Michael Grinfeld, in the December 1998 California Lawyer, opens several doors. Grinfeld notes that “in the past year nearly a dozen cases involving Prozac have disappeared from the court record.” He is talking about law suits against the manufacturer, Eli Lilly, and he is saying that these cases have apparently been settled, without trial, in such a quiet and final way, with such strict confidentiality, that it is almost as if they never happened.

This smoothness, this invisibility keeps the press away and also, most importantly, does not encourage other people to come out of the woodwork with lawyers and Prozac horror-stories of their own. Because they are not reading about $2 million or $10 million or $50 million settlements paid out by Lilly.

Grinfeld details a set of maneuvers involving attorney Paul Smith, who in the early 1990s became the lead plaintiffs’ counsel in the famous Fentress case against Eli Lilly. The case made the accusation that Prozac had induced murder. This was the first action involving Prozac to reach a trial and jury, so it would establish a major precedent for a large number of other pending suits against the manufacturer.

After what many people thought was a very weak attack on Lilly by lawyer Smith, the jury came back in five hours with an easy verdict favoring Lilly and Prozac.

Grinfeld writes, “Lilly’s defense attorneys predicted the verdict would be the death knell for [anti-]Prozac litigation.”

But that wasn’t the end of the Fentress case, even though Smith-to the surprise of many-didn’t appeal it. “Rumors began to circulate that Smith had made several [prior] oral agreements with Lilly concerning the evidence that would be presented [in Fentress], the structure of a postverdict settlement, and the potential resolution of Smith’s other [anti-Prozac] cases.”

In other words, the rumors said: This lawyer made a deal with Lilly to present a weak attack, to omit evidence damaging to Prozac, so that the jury would find Lilly innocent of all charges. In return for this, the case would be settled secretly, with Lilly paying out monies to Smith’s client. In this way, Lilly would avoid the exposure of a public settlement, and through the innocent verdict would discourage other potential plaintiffs from suing it over Prozac.

The rumors congealed. The judge in the Fentress case, John Potter, asked lawyers on both sides if “money had changed hands.” He wanted to know if the fix was in. The lawyers said no money had been paid, “without acknowledging that an agreement was in place.”

Judge Potter didn’t stop there. In April 1995, Grinfeld notes, “In court papers, Potter wrote that he was surprised that the plaintiffs’ attorneys [Smith] hadn’t introduced evidence that Lilly had been charged criminally for failing to report deaths from another of its drugs to the Food and Drug Administration. Smith had fought hard [during the Fentress trial] to convince Potter to admit that evidence, and then unaccountably withheld it.”

In Judge Potter’s motion, he alleged that “Lilly [in the Fentress case] sought to buy not just the verdict, but the court’s judgment as well.”

In 1996, the Kentucky Supreme Court issued an opinion on all this: “… there was a serious lack of candor with the trial court [during Fentress] and there may have been deception, bad faith conduct, abuse of the judicial process or perhaps even fraud.”

After the Supreme Court remanded the Fentress case back to the state attorney general’s office, the whole matter dribbled away, and then resurfaced in a different form, in another venue. At the time of the California Lawyer article, a new action against Smith was unresolved.

If Lilly went to extreme lengths to control suits against Prozac, it stands to reason that drug companies could also try to deflect legal actions by influencing how the press, lawyers, and public view these school shootings. For example, accusing video games is acceptable, accusing guns is acceptable, accusing bad parents is acceptable. In fact, these causes, as I stated above, are legitimate. But when the national press is completely silent on medical drugs, we have to question the background on that. We have to. We have to ask, why should THIS horrendous factor be eliminated altogether from reporting to the nation?

The PBS television series, The Merrow Report, produced in 1996 a program called “Attention Deficit Disorder: A Dubious Diagnosis?” The Educational Writer’s Association awarded the program first prize for investigative reporting in that year. I can recall no other piece of television journalism since the Vietnam war which has managed to capture on film government officials in the act of realizing that they have made serious mistakes.

John Merrow, the series’ host, explains that, unknown to the public, there has been “a long-term, unpublicized financial relationship between the company that makes the most widely known ADD medication [Ritalin] and the nation’s largest ADD support group.”

The group is CHADD, based in Florida. CHADD stands for Children and Adults with ADD. Its 650 local chapters sponsor regional conferences and monthly meetings-often held at schools. It educates thousands of families about ADD and ADHD and gives out free medical advice. This advice features the drug Ritalin.

Since 1988, when CHADD and Ciba-Geigy (now Novartis), the manufacturer of Ritalin, began their financial relationship, Ciba has given almost a million dollars to CHADD, helping it to expand its membership from 800 to 35,000 people.

Merrow interviews several parents whose children are on Ritalin, parents who have been relying on CHADD for information. They are clearly taken aback when they learn that CHADD obtains a significant amount of its funding from the drug company that makes Ritalin.

CHADD has used Ciba money to promote its pharmaceutical message through a public service announcement produced for television. Nineteen million people have seen this PSA. As Merrow says, “CHADD’s name is on it, but Ciba Geigy paid for it.”

It turns out that in all of CHADD’s considerable literature written for the public, there is rare mention of Ciba. In fact, the only instance of the connection Merrow could find on the record was a small-print citation on an announcement of a single CHADD conference.

In recounting CHADD’s promotion of drug “therapy” for ADD, Merrow says, “CHADD’s literature also says psychostimulant medications [like Ritalin] are not addictive.”

Merrow brings this up to Gene Haslip, a Drug Enforcement Agency official in Washington. Haslip is visibly annoyed. “Well,” he says, “I think that’s very misleading. It’s [Ritalin’s] certainly a drug that can cause a very high degree of dependency, like all of the very potent stimulants.”

Merrow reveals that CHADD received a $750,000 grant from the US Dept. of Education, in 1996, to produce a video, Facing the Challenge of ADD. The video doesn’t just mention the generic name methylphenidate, it announces the drug by its brand name, Ritalin. This, at government (taxpayer) expense.

We see a press conference announcing the release of the video. The CHADD president presents an award to Dr. Thomas Hehir, Director of Special Education Programs at the US Dept. of Education.

This sets the stage for a conversation between Merrow and Dr. Hehir, providing a rare moment when discovery of the truth is recorded on camera, when PR is swept aside.

MERROW: “Are you aware that most of the people in the film [the video, Facing the Challenge of ADD-referring to people who are giving testimonials about how their ADD children have been helped by treatment] are not just members of CHADD … but in the CHADD leadership, including the former national president? They’re all board members of CHADD in Chicago. Are you aware of that? They’re not identified in the film.”

HEHIR: “I’m not aware of that.”

MERROW: “Do you know about the financial connection between CHADD and Ciba Geigy, the company that makes Ritalin?”

HEHIR: “I do not.”

MERROW: “In the last six years, CHADD has received $818,000 in grants from Ciba Geigy.”

HEHIR: “I did not know that.”

MERROW: “Does that strike you as a potential conflict of interest?”

HEHIR: “That strikes me as a potential conflict of interest. Yes it does.”

MERROW: “Now, that’s not disclosed either. Even though the film talks about Ritalin as a-one way, and it’s the first way presented-of taking care of treating Attention Deficit Disorder. That’s not disclosed either. Does that trouble you?”

HEHIR: “Um, it concerns me.”

MERROW: “Are you going to look into this, when you go back to your office?”

HEHIR: “I certainly will look into some of the things you’ve brought up.”

MERROW: “Should they have told you that all those people in that film are CHADD leadership? Should they have told you that CHADD gets twenty percent of its money from the people who make Ritalin?”

HEHIR: “I should have known that.”

MERROW: “They should have told you.”

HEHIR: “Yes.”

This funded video, in which CHADD devotes all of twenty seconds to mentioning Ritalin’s adverse effects, is no longer distributed by the US Department of Education.

CHADD has now told its members that it receives funding from Ciba. It says it will continue to take money from Ciba.

This is an example of how a corporation can, behind the scenes, bend and shape the way the public sees reality.

In the case of the school shootings, has an attempt been made to mold media response? To highlight various causes and omit others?

Real action is going to have to come from the public. Mothers in Littleton and Springfield and West Paducah and Jonesboro are going to have to ask the hard questions and become relentless about getting real answers. They are going to have to learn about these drugs. They’ll have to learn which violent children in the school shootings were on these drugs. They are going to have to throw off robotic obedience to authorities in white coats. And they are going to have to join together.

If they do, many people will end up standing with them.

POSTSCRIPT (circa 2001)

Since this inquiry was published in early May 1999, I have had requests to include more information about Ritalin. Mothers have told me they need whatever they can get their hands on, in order to deal with teachers, school principals, school boards, and government agencies who are determined to force Ritalin on their children.

To begin with, I would suggest that these concerned and embattled parents write letters to many medical and psychiatric and law-enforcement officials of high standing, asking for a definitive answer to the questions: Is it legal to pressure us with threats? Can my child be kept out of school if I refuse Ritalin? A background of on-the-record No’s can be used to enlighten the ignorant.

Let’s start with the first listed symptoms of the condition officially named Attention Deficit Hyperactivity Disorder (ADHD).* For this I am consulting the DSM-IV, the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, published by the American Psychiatric Association.

[ *In a domain of embarrassingly crude definitions, ADHD and ADD (Attention Deficit Disorder) are more or less equivalent. ADHD is the larger, more opulent land-vehicle which has replaced the older mini-van, ADD. ]

“Individuals with this disorder [ADHD] may fail to give close attention to details or may make careless mistakes in schoolwork or other tasks (Criterion A1a).”

“Work is often messy and performed carelessly and without considered thought… (Criterion A1b).”

“They [students] often appear as if their mind [sic] is elsewhere or as if they are not listening or did not hear what has just been said (Criterion A1c).”

The reader immediately assumes that, although these symptoms are vague and could stem from many reasons on many different days of the week, the whole business must somehow be attached to a central underpinning, one thing from which the diverse behaviors arise, like debris floating on the sea from a ship that has already sunk.

But, staying with the DSM-IV, under a nearby section called “Associated laboratory findings,” we read: “There are no laboratory tests that have been established as diagnostic in the clinical assessment of Attention-Deficit Hyperactivity Disorder.”

So although behaviors are offered as signs of ADHD, no organic cause is named.

Despite that, an official psychiatric disorder, ADHD, has, in the absolutely official DSM-IV, been catalogued and presented as needing medication.

But without a central cause, basic logic dictates, there is no assurance of a Disorder.

Comes then, in the DSM-IV, a sub-category of ADHD called Conduct Disorder, the invention of which, as a “disease,” communicates a degree of utter fabrication that is stunning.

“The essential feature of Conduct Disorder is a repetitive and persistent pattern of behavior in which the basic rights of others or major age-appropriate societal norms or rules are violated. These behaviors fall into four main groupings: aggressive conduct that causes or threatens physical harm to other people or animals (Criteria A1-A7), non-aggressive conduct that causes property loss or damage…”

Again, no cause. No microorganism, no chemical imbalance, no brain malfunction. Just a bald kidnapping of certain kinds of bad behavior under the title of “medical problem.”

“What we have here is an illness.”

“Really? What’s the cause?”

“Well… we don’t know.”

“Then how do you know it’s an illness?”

“Because people have it.”

“Have it?”

“Yes.”

“You mean they behave in various ways.”

“Well…”

Conduct Disorder is superseded in transparency only by another ADHD category, Oppositional Defiant Disorder.

Why not form up an infant condition called Frowning and imply it has a single invariable biological root?

There are gentle members of our society who pray and believe that the authorities really do have a clue because they simply must. Because otherwise the whole so-called mental health edifice might come crashing down around our ears.

In the gold-plated PDR, the Physician’s Desk Reference for 1999, under the drug Ritalin (methylphenidate), we are cautioned: “Specific etiology (causation) of this syndrome [ADHD] is unknown, and there is no single diagnostic test.”

Again. Define a disease without knowing what causes it. And, give a drug (Ritalin) for it.

To know that something is a disease is to know the cause.

Otherwise, and certainly as time goes on, you cannot say you have a disease at all. You can only say you have a series of loosely connected or similar behaviors or symptoms, and you suspect there may be a single agent bringing them all about. You have a feeling. You have a hunch. A premonition. Faith.

On that basis, should over two million American children be treated with Ritalin for ADHD?

The 1999 PDR states, “Sufficient data on safety and efficacy of long-term use of Ritalin in children are not yet available.” That is a staggering remark. Particularly on the safety side.

The first tier of adverse effects listed for Ritalin in the PDR includes: nervousness, insomnia, hypersensitivity (including skin rash), fever, necrotizing vasculitis, anorexia, nausea, dizziness, palpitation, dyskinesia, tachycardia, angina, cardiac arrhythmia. These effects are rounded out by Tourette’s syndrome and toxic psychosis.

Again, Goodman and Gilman’s The Pharmacological Basis of Therapeutics states that Ritalin is “structurally related to amphetamines… Its pharmacological properties are essentially the same as those of the amphetamines.”

A parent said to me, “You mean the doctor is prescribing speed for my son?”

I referred her to the above quote a number of times. Perhaps with sufficient chanting of it she will finally get the message.

Any drug counselor can tell you about speed: it makes some people feel better for a little while. Your head clears up. You function more clearly. You have confidence. Then that all disintegrates and you slowly or quickly crash. You develop very negative symptoms. (See Scarnati above.)

This is not complicated. Ritalin is speed dressed up as a medicine. Users frequently go on to other drugs to even themselves out. They become aggressive, they have physical problems.

One parent told me her doctor assured her that “many children are helped by Ritalin.” When she asked him for names and statistics he smiled and said, “I’m not in the business of supplying proof to every question. I wouldn’t have time to practice medicine.” She continued to press him. She asked him if he was aware that the PDR cannot offer proof of the safety of Ritalin over the long-term. He said, “What do you want me to do?” “Not give the drug,” she said. He promptly ended the conversation. It not being on the clock.

For some people, the corporation itself, the manufacturer of a pharmaceutical, is the ultimate referral point, the final back-up for believing in the safety and efficacy of the drug. Along with the FDA, which is held inviolate by many, the company emanates an aura of honorable purpose. As in, how could a drug corporation spend decades turning out these medicines if they weren’t Good?

The original patent-holder and principal manufacturer of Ritalin is Ciba-Geigy, whose headquarters are in Switzerland. C-G is now Novartis, having merged with Sandoz, but I shall continue to call the company Ciba, for historical purposes.

In addition to my comments above on CHADD, the Ciba-financed ADHD support-group, let’s take this a little further. Has Ciba ever been involved with another drug which was shown to have profoundly negative effects? In other words, should the corporation’s prior reputation inspire naive faith?

In the autumn of 1970, the Japanese government banned the use of all medical drugs in Japan which contained the compound called clioquinol. These antidiarrheal medications were manufactured under a variety of names by Ciba.

More than 11,000 people in Japan had suffered from the effects of clioquinol between 1955 and 1970. Some of the symptoms: numbness, blindness, paralysis, death.

There was a smokescreen between clioquinol and the Japanese discovering that the drug was the cause of what was being called subacute myelo-optic neuropathy (SMON). The medical establishment was bent in the direction of looking for germs.

Eventually, through the courageous work of several researchers and a lawyer, the truth was exposed.

But Ciba knew as early as 1935 that there were serious problems with clioquinol. Reports had come in from Argentina, where the compound was introduced as an oral preparation for the first time. The same symptoms which much later surfaced in Japan were being cited in Argentina.

Animal tests – as misleading as they are – are relied on by pharmaceutical companies. In the case of clioquinol, Ciba found in the late 1930s that cats were convulsing and sometimes dying from the drug. Dogs were dying from seizures.

Dr. Olle Hanson, a Swedish researcher, published a paper in The Lancet in 1966, linking optic atrophy and blindness to clioquinol.

Ciba did nothing.

Victims of the drug in Japan began to sue Ciba in 1972. It took 6 years to wring an apology and dollar damages out of the company.

Yet Ciba issued a press release in 1980 on SMON, saying “there is no conclusive evidence that clioquinol causes SMON.” In fact, the company continued to manufacture and sell drugs containing clioquinol in other countries.

Ciba dragged its feet until 1985, at which time it stopped manufacturing clioquinol for oral use. (This piece of history about clioquinol and Ciba comes from several sources, including the excellent information gathering organization, Health Action International, based in Amsterdam, and one of its lead writers, Andrew Chetley.)

With ADHD, the developing premise that there was one condition at the heart of all the symptoms was the error. It is an error that is made every day in hundreds of labs around the world. Begin from the other end. Jimmy is fidgety. He can’t sit still in class. He yells when he should be quiet. He draws elephants when he should be adding numbers. He walks around when he should sit down. He does cartwheels in the hall.

Imagine a good doctor interviewing Jimmy. For several hours, perhaps, over several appointments. He wants to know all about the boy. Is he bored? Is he feeling nervous in school? Is there someone he’s afraid of? Is there a subject he really wants to study that is not being offered? Does he have a buried talent? Is he eating various junk foods that contain chemicals and preservatives which might be producing anxiety? Does he have serious allergies? Are his parents absent or abusive? And so on down the list, a very long list.

I have been told of several instances of so-called ADHD resolved when, for example, correct changes were made in the foods and nutrients children ate.

To this claim, psychiatrists often say, “That’s ridiculous. Nutrition has nothing to do with it, because ADHD is a brain malfunction.” Of course that is arrogantly begging the question, and the same arrogance can be gleaned simply by opening up the DSM-IV and reading the sentences about ADHD. They are rife with deductions based on unproven assumptions, all concocted at a great emotional distance from children.

No, it’s one child at a time. One child at a time. That’s the way to be a decent human being and a decent practitioner, instead of talking nonsense from a very high cathedral.

There are enough relentless mothers of children out there to open up new land, to change the damaging way this whole business is being handled. And in the process, they might make Ciba and other similar entities pay dearly for their misdeeds.

As one doctor has written, if a school official or doctor says that your child must take Ritalin because he has ADHD, you have the right to demand proof that ADHD is a disease in the first place. You have a right to demand such proof all the way down the line, without backing away, without buying bland assurances or arrogant threats from “highly educated experts.” You have the right to state that the doctor in question is stepping over the line into violating informed consent statutes, because those laws insist that the patient is told the whole truth about what is going to be done to him and why. You have the right to say the demand that your child take Ritalin is an instance of medical malpractice.

It is your choice.

It always is.

What follows is based on a series of conversations between educated mothers and their doctors about Ritalin and ADHD. I’ve paraphrased the mothers’ reports and telescoped them into one short conversation.

“My son needs medicine?”

“Yes. Ritalin. He has ADHD.”

“But I understand there is no proof that ADHD is a disease.”

“We know it’s a chemical imbalance in the brain.”

“You do?”

“Yes.”

“How?”

“Through research.”

“But I’ve read that no definite cause has been found.”

“We’re still looking for that.”

“So it might be something else. My son might have problems that come from another source.”

“No, he has ADHD.”

“I’ve read the definition of ADHD in the DSM-IV. It’s a list of behaviors. They might come from a lot of different causes.”

“Who have you been talking to?”

“I’ve been reading.”

“ADHD is a disease.”

“A disease has a cause, Doctor. Otherwise there’s no way of knowing it’s one disease.”

“It takes time to learn all about diseases.”

“No. You have to know the cause. Otherwise you don’t know you have a disease to begin with. My son could be hyperactive because of a hundred things. He could have allergies.”

“That’s ridiculous.”

“Why?”

“There isn’t any literature on that.”

“I’ve talked to a number of health practitioners, and they tell me in some cases allergies caused the hyperactivity.”

“Rarely. Your son has ADHD. It’s like any other disease. Diabetes, for example. He needs medicine.”

“Nonsense. And besides, Ritalin is speed.”

“It’s a medicine.”

“I don’t want my son treated with it.”

“You’re being negligent.”

“According to what?”

“The psychiatric research on this subject.”

“I have research that says ADHD is not a disease and that Ritalin can have very harmful effects.”

“You’re being resistent.”

“No, I’m being careful. It’s my son’s life. You want to tell him that he has a malady and that his brain is involved. That’s going to give him the idea that something is wrong with him. That he’s less than normal. I won’t let you do that unless you can show me the exact place where it says Ritalin is caused by a particular thing. I know you can’t show me that.”

“You’re being stubborn. You can’t just walk away from this.”

“Giving him Ritalin is walking away from it.”

“You know, the reason there are doctors is because we have skills and knowledge about these things. You don’t.”

“I’ve read enough of the literature. I can understand it when no cause is given, when a bunch of behaviors are suddenly labeled a disease. That’s bad medicine.”

“We’re getting nowhere.”

“You should go back to the basic literature on ADHD. It’s made up of words that show no real proof. It’s my son. Until you can show me that ADHD has an organic cause, and that Ritalin cures that, or changes it for the better, you won’t get my okay.”

“You’re causing your son harm by this attitude.”

“No, I’m protecting him.”

“The people in charge at his school won’t think that. They’ll be very upset.”

“So I should give in to them because they’re upset? I don’t think so.”

“They might not let your son back in school.”

“Then I’ll sue them and anyone else who contributes to that decision.”

“You’d be up against very powerful people.”

“I’m not raising my son to be a coward, and I won’t be one either.”

“You know, most parents agree to treatment immediately.”

“They’re relieved about avoiding any involvement, any responsibility. Or they’re just relieved to hear a doctor say it isn’t their fault. They’re tired and worn out and they want a pill to do the job. I know fifty kids at school who are on Ritalin, and I know things their parents could be doing as parents that would calm their kids down. Without drugs. In some cases that means being better parents. In some cases it means exploring their environment.”

“Environment? What does that mean?”

“Chemicals that disturb the functioning of the body and the nervous system. Toxins, pollutants, chemicals in the food. Allergies. Lots of things.”

“No research points to those as the cause of ADHD.”

“Because the research I’m talking about isn’t usually carried on under the banner of ADHD. ADHD is just a name. It’s very misleading and has caused a lot of confusion…”

“You’re a troublemaker.”

“Listen, Doctor, this comes down to a question of rights. Do I have the right, the civil and human right to refuse Ritalin for my child. I’m informed. I’m aware. I’m not stupid. It’s my choice, regardless of what you think.”

One of the mothers told me she was “referred” for psychological counseling because she refused to allow Ritalin for her child. This referring was done by her child’s pediatrician. The mother refused the counseling.

So to summarize: over a period of years, psychiatrists doing “research” collect child behaviors and assemble them into an interlocking list. They call this list ADHD, although no cause has been found, and they determine that a drug whose properties are essentially the same as amphetamine, Ritalin, should be used to treat the disease. When a parent refuses to allow the drug to be given, he or she may be referred for counseling. This “therapy” would presumably involve digging up the “real reasons” for the parent’s resistance. What is the parent harboring that prevents him/her from wanting the child to get better? Or, to put it another way, how can “licensed professionals” convince a parent to abandon all semblance of rationality and pretend that, deep down, the desire to protect a child from a dangerous drug is really a neurosis, a phobia, a fragment of pathology perhaps itself requiring medication?

Which proves that not all cold-blooded species live out of town.

As this postscript goes to press, we read in the May 22nd New York Times that T. J. Solomon, Jr. the boy who wounded several of his classmates at a suburban Atlanta school, was on Ritalin. Treated for depression, he was possibly also on one of the SSRIs, such as Prozac or Zoloft.

And Phil Hartman’s brother, the executor of the dead actor’s estate, has just filed a suit against Pfizer, the manufacturer of Zoloft. Brynn Hartman who murdered her husband a year ago, was being treated for depression by Los Angeles psychiatrist Arthur Sorosky with Zoloft.

Some sources of information (may no longer be operating in 2012):

Dr. Peter Breggin, psychiatrist, author, former full-time consultant with the National Institute of Mental Health. www.breggin.com 

ICSPP News. Phone: 301-652-5580 www.icspp.org

Dr. Joseph Tarantolo, psychiatrist, president of the Washington chapter of the American Society of Psychoanalytic Physicians. Phone: 301-652-5580

The Merrow Report can be ordered by phone at 212-941-8060.

The ICSPP News publishes the following warning in bold letters: “Do Not Try to Abruptly Stop Taking Psychiatric Drugs. When trying to withdraw from many psychiatric drugs, patients can develop serious and even life-threatening emotional and physical reactions… Therefore, withdrawal from psychiatric drugs should be done under clinical supervision…”

ADHD Action Group: 212-769-2457

Many thanks to Dr. Peter Breggin. Much information in this article was obtained through his landmark book, Toxic Psychiatry.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at NoMoreFakeNews.com or OutsideTheRealityMachine.

FDA LUNATICS AND CRIMINALS

 

FDA LUNATICS AND CRIMINALS

 

AUGUST 5, 2011. In a 2010 action filed against the FDA, the Farm-to-Consumer Legal Defense Fund sought to protect the freedoms and rights of family farms—particularly when it came to the right to ship raw milk across state lines.

 

The FDA responded to that filing in a most revealing way. In an astonishing way. Its position allows you to see into its bureaucratic/fascist soul, if an agency can be said to have a soul.

 

Read these words (from FDA) carefully, because they amount to a manifesto and a prediction about what is to come, if the people of this country don’t push back in overwhelming numbers:

 

Plaintiffs assertion of a ‘fundamental right to their own bodily and physical health, which includes what foods they do and do not choose to consume for themselves and their families,’ is simply unavailing because plaintiffs do not have any fundamental right to obtain any food they wish.”

 

And then the FDA made this assertion:

 

There is no fundamental right to freedom of contract.”

 

After you pick yourself up off the floor, think about why the FDA made the latter statement.

 

Small farms and consumers have been forming clubs in America, just like the club, Rawesome Foods, that was raided two days ago. These private groups are created to engage in contracts, agreements among themselves, about what foods they will buy and sell.

 

In the case of raw milk, in order to avoid interference by the government, the club members agree to take responsibility for their own health, and the consequences, if any, of drinking raw unpasteurized milk.

 

They are, in effect, saying, “We make the choice. The choice doesn’t involve the government, one way or another. This is a private contract.”

 

But the FDA steps in and issues their edict: you don’t have a fundamental right to a contract. You especially don’t have a right to a contract that contravenes one of our regulations. You are under US. We decide, not you.

 

Those are the battles lines. They have been drawn in stark terms. The federal government isn’t going to change. It needs to be able to obliterate any private agreement in order to expand its control. It needs to be able to say, YOU ARE NOT A GOVERNMENT BY THE PEOPLE, YOU ARE A PEOPLE BY THE GOVERNMENT.

 

In these FDA comments, which deserve to be communicated far and wide so people can understand what is being done to them, the federal government has let its share-and-care mask drop, and has shown its face.

 

Look at it.

 

JON RAPPOPORT

www.nomorefakenews.com

qjrconsulting@gmail.com

When the Blood Boils: Vaccines and Autism

by Jon Rappoport

July 2, 2011

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Lies passed around like conjured pieces of gold. Medical liars speaking their messages with straight faces, from their pulpits of influence.

We’ve watched them work. We’ve experienced the inner sensation of blood boiling; outrage.

Who are these people? Where did they come from? How did they attain their positions of power? Are they a different species?

And like you, I have watched the passive faces of audiences as they take in these lies, as they know something is wrong, as they refuse to act.

If you control the meaning of words like “evidence,” “cause,” “relationship between,” you own the playing field. You can manipulate outcomes and conclusions, and you can define science itself.

Your power derives from ownership of those simple words.

Suppose a healthy baby with all his faculties intact receives a barrage of vaccines at 15 months. Then, three days later, his temperature soars to 105, he has seizures, he screams, and then he goes silent. He withdraws from the world, from his parents. In the ensuing months, he doesn’t speak. He doesn’t laugh. He shows no interest in life around him. He doesn’t recover from this. He doesn’t regain his former health.

In what sense can it be said that the vaccines caused his condition? That may seem like an absurd question to be asking, but scientists claim it is important. So do judges and government officials. So do drug companies who make and sell vaccines.

They claim it’s very important, because they want to maintain control over the concept of “cause.” It’s their protection in the racket they are running.

Can we track the path, step by step, of these vaccine ingredients as they are injected into a baby and make their way through his system? Can we observe every reaction they produce, in sequence, all the way into and through the recesses of the nervous system and the brain?

Of course not.

By such an impossible standard, everyone falls short.

If perverse officials and scientists suddenly invoke that standard, can anyone fulfill it? No.

But make sure you understand that scientists and bureaucrats judge their own work by far looser principles.

They assert, for example, with psychotic arrogance that the underlying cause of autism is in the genes, although their research has only given them the foggiest of reasons for even beginning to crawl out on that limb—where they crow and lie and ask for more research money.

They say ADHD is created by certain brain abnormalities, even though their scans produce on-again off-again evidence—which, finally, is no evidence at all.

In fact, for every one of the 297 so-called mental disorders that are named and defined and described in the official bible of psychiatric literature, there is not one, not one lucid diagnostic test to back up, biologically, their disease labels and descriptions and definitions.

It’s a game. “We may hold you to an impossible standard. We hold ourselves to no standard at all.”

So you should be aware that, if you choose to enter this game, for whatever reasons, you are playing against a monumentally stacked deck.

The powers-that-be will do everything they can to subvert, deny, and destroy THE STORY OF ONE PARENT ABOUT ONE CHILD.

Why? Because the story is too convincing. It’s too obvious. It’s too real. It’s too DEVASTATING. It’s too dangerous.

“My child was healthy. He was vaccinated. Then he collapsed. He never recovered.”

With that, you are setting dynamite on the rails of the medical princes.

And you are also waking up other parents whose stories are essentially the same. You are igniting a fire in their heads.

Can you imagine what would happen if you said, “Look, my child was hit by a cluster of vaccines delivered when he was fifteen months old, and he was never the same after that, and THAT is what I’m seeking compensation for, and that is ALL I’m seeking compensation for. I don’t care what you call it, what name you give to it.”

And the government said, “Well, all right.”

The ensuing flood would drown them. And would drown the vaccine manufacturers, too.

You must be stopped.

And the way they will stop you is by manipulating the word “cause.” That’s all. That’s their entire policy and program. They execute it on an arcane and pseudo-technical level, employing models and constructs and numbers in their private little universe, while they polish their credentials.

They don’t want YOUR STORY to stand naked in front of the public.

Of course it is obvious that, when health turns to tragedy, the vaccines were at fault, just as when a blow to the head causes memory loss. Of course everyone concerned knows the truth.

But they say: science is not done this way. We must have “evidence of causation.” They occasionally throw a few crumbs to parents whose child was brain-damaged by a vaccine. But in the main, they conjure up a version of pseudo-science and use it to obfuscate the otherwise unpardonable reality of what the vaccine has done.

And how does this conjured and manufactured science work?

It starts with the owned and operated definition of a disease or disorder. In the case of autism, the old behavioral criteria are dragged out. Here they are. I’m sorry for loading the full display on you, but I want you to see it in print:

The following is from Diagnostic and Statistical Manual of Mental Disorders: DSM IV

(I) A total of six (or more) items from (A), (B), and (C), with at least two from (A), and one each from (B) and (C)

(A) qualitative impairment in social interaction, as manifested by at least two of the following:

1. marked impairments in the use of multiple nonverbal behaviors such as eye-to-eye gaze, facial expression, body posture, and gestures to regulate social interaction
2. failure to develop peer relationships appropriate to developmental level
3. a lack of spontaneous seeking to share enjoyment, interests, or achievements with other people, (e.g., by a lack of showing, bringing, or pointing out objects of interest to other people)
4. lack of social or emotional reciprocity ( note: in the description, it gives the following as examples: not actively participating in simple social play or games, preferring solitary activities, or involving others in activities only as tools or “mechanical” aids )

(B) qualitative impairments in communication as manifested by at least one of the following:

1. delay in, or total lack of, the development of spoken language (not accompanied by an attempt to compensate through alternative modes of communication such as gesture or mime)
2. in individuals with adequate speech, marked impairment in the ability to initiate or sustain a conversation with others
3. stereotyped and repetitive use of language or idiosyncratic language
4. lack of varied, spontaneous make-believe play or social imitative play appropriate to developmental level

(C) restricted repetitive and stereotyped patterns of behavior, interests and activities, as manifested by at least two of the following:

1. encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus
2. apparently inflexible adherence to specific, nonfunctional routines or rituals
3. stereotyped and repetitive motor mannerisms (e.g hand or finger flapping or twisting, or complex whole-body movements)
4. persistent preoccupation with parts of objects

(II) Delays or abnormal functioning in at least one of the following areas, with onset prior to age 3 years:

(A) social interaction
(B) language as used in social communication
(C) symbolic or imaginative play

(III) The disturbance is not better accounted for by Rett’s Disorder or Childhood Disintegrative Disorder

And now you have the full and complete definition of autism from the official manual. There is no other definition. There are no physical tests or blood tests or brain scans. There is only this menu of behaviors.

And there are many so-called related disorders, and each one has its similar complex behavioral definition. These depictions overlap. But no matter. As far as the psychiatrists and pediatricians and medical bureaucrats are concerned, autism is defined. Engraved on tablets.

Does, in the judgment of a doctor, your child fit the definition or doesn’t he? The word is given from on high. The decision is rendered. And we are then one step removed from the reality of the simple and brutal destroying effects of the vaccines. This is good for them. They are now in familiar territory. Protected land.

Now they can say, “Your child, who at fifteen months collapsed, has autism.”

This is the bridge to the next giant step. Which is:

“We have determined that vaccines are not the cause of autism.”

“We know this.”

“We have proved this.”

Therefore, you’re trapped. Your child has been painted with the label “autism”–and perhaps you were actually hoping for that, because you knew something was terribly wrong, and the designation confirms you were correct. But as far as making a link to the vaccines, you’re suddenly at their mercy.

If they decide to compensate you through the federal vaccine compensation system, they will say, “Well, your child actually is suffering from encephalopathy and has autism-like symptoms.” But far more frequently, they will fall back on their pronouncement that vaccines and autism are unconnected, and you will get nothing.

How did these medical experts and their bureaucratic partners determine that vaccines are not the cause of autism?

They examined studies. And the studies “found no link.” In particular, there is the key Verstraeten study, published in two phases. Three HMOs’ records of babies were considered by Verstraeten and his colleagues.

I’m going to quote from the study and then comment:

“Results. In phase I at HMO A, cumulative exposure at 3 months resulted in a significant positive association with tics (relative risk [RR]: 1.89; 95% confidence interval [CI]: 1.05–3.38). At HMO B, increased risks of language delay were found for cumulative exposure at 3 months (RR: 1.13; 95% CI: 1.01–1.27) and 7 months (RR: 1.07; 95% CI: 1.01–1.13). In phase II at HMO C, no significant associations were found. In no analyses were significant increased risks found for autism or attention-deficit disorder.”

“Conclusions. No consistent significant associations were found between TCVs and neurodevelopmental outcomes. Conflicting results were found at different HMOs for certain outcomes. For resolving the conflicting findings, studies with uniform neurodevelopmental assessments of children with a range of cumulative thimerosal exposures are needed.”

First of all, notice how far away we are from that basic fact that vaccines were delivered to your child and your child collapsed and never recovered. We are miles from that. We’re now discussing correlations between vaccines containing mercury (thimerosal) and various indicators and labels: tics, language delay, autism, attention-deficit disorder, neurodevelopmental outcomes.

We now have a complex situation. First of all, in order to conclude that mercury-containing vaccines are correlated with autism or attention-deficit disorder, the researchers would have to have observed, in these children’s medical records, reports detailing all the behavioral criteria THE RESEARCHERS ASSUME add up to a positive diagnosis of these two INVENTED disorders—neither of which even exists on the basis of actual biological or chemical tests of any kind.

So essentially, if we make the translation from psychiatric-speak to basic English, we have this: “There is no convincing correlation between mercury-containing vaccines and those disorders we invented by slicing and dicing human behavior into compartments and giving them disease-labels.”

This is staggering when you think about it.

Continuing: In the first HMO records, Verstraeten and his colleages found a significant correlation between the vaccines and tics. As in facial tics. Why is that important? Because tics can be a sign of motor brain damage. They have a name for that: tardive dyskinesia. But it means brain damage.

However, if you look at the concocted definitions of the concocted disorders called autism and ADD, you’ll find no mention of tics or tardive dyskinesia. Therefore, an increased risk of tics doesn’t bring the researchers any closer to connecting vaccines and autism—simply because autism wasn’t defined that way. It wasn’t invented that way.

Perusing the records at the second HMO, Verstraeten found an increased risk of language delay. The babies didn’t start speaking when normally expected to. This is one of the listed criteria for a diagnosis of autism, but of course it is not enough, by the concocted rules of the game, to rate a placing of the invented label, autism, on any of those children.

At the third HMO, which was investigated as a separate phase 2 of the study, researchers found no significant associations—meaning no tics, no language delay…nothing that would rate a diagnosis of autism or suggest the presence of any of the invented symptoms of autism.

All in all, Verstraeten and his colleagues found no reason to conclude that mercury-containing vaccines were correlated with autism or other signals of neurological problems.

He played off one HMO against another: “In this one, we found X. But in the other one, we didn’t. We found Y instead. And in the third one, we found neither X nor Y.” Why didn’t he simply use all three HMOs as one reservoir? Possibly because he was trying to guard against the possibility of biased records at one HMO. Who knows?

And why didn’t he conclude, “All in all, we discovered some evidence of harm from the vaccines.”

Again, notice how far we are from the actual event of vaccines causing brain damage in a child.

The study decides that there is no increased risk, from vaccines, for autism or ADD. And that’s that. “Further research” is needed.

A child harmed by vaccines could have a tiny brain lesion or severe immune deficiency or a rewired connection somewhere deep in the recesses of the brain—undetected—but none of this matches up to the invented criteria for a diagnosis of autism.

But millions of people actually believe that autism is a distinct entity which was “discovered,” like a pre-set embedded pattern of errant pathways in the brain. And when those people are told, by experts, that vaccines don’t cause it, the PR value is enormous. For doctors who give the vaccines, for drug companies, for public-health agencies.

This is all a ruse. It’s a fabrication, and the studies that follow from it serve to mask the facts of vaccine damage.

They invent define the disorder, they have no definitive diagnostic tests for it, they conclude that vaccines don’t cause it. It’s one fantasy after another.

It’s as if you drew a map of a gold mine that doesn’t exist, and then you passed a law forbidding people from searching for it.

There are various degrees and events of tragic and lasting impact-damage that are laid upon children. The causes are multiple. One significant cause is vaccines. There is no such thing as autism. It is a construct ultimately designed to get certain people off the hook. And to make profit. And to engender money for research.

They will never find a cure for autism, because it doesn’t exist, except as a menu of behaviors wrapped inside their fantasy. Of course, if they were in the world, the world you live in, they would acknowledge that vaccines do cause brain and neurological damage, and they would compensate for that. They would act in a straightforward and honest fashion.

I spoke to one psychiatrist off the record, who said, “A genetic cause for autism? Are you serious? Autism is an artifact to begin with. So how do you find a gene that causes a fairy tale?”


The Matrix Revealed

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)


Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

BIGGEST BULLSHITTER IN AMERICA?

Biggest bullshitter in America? Who is Dr. Allen Frances?

by Jon Rappoport

June 30, 2011

www.nomorefakenews.com

Hey, the man may be a saint. Who knows? He might be so far beyond my ability to comprehend him I can’t hope to grasp the meaning of his work. He might deserve a Nobel Prize and the thanks of a grateful nation and a statue in the Smithsonian. But…

Is it possible this doctor is the biggest bullshitter in America? I’m just asking, because I’ve been thinking about running a contest. Also because I’ve been reading the interesting statements he made to Gary Greenberg, author of a Wired article: “Inside the Battle to Define Mental Illness.” (Dec.27, 2010).

How that article failed to make it out into the mainstream and grab big headlines is beyond me. Well, not really, given its incendiary implications. Editors and reporters at major media outlets have an uncommon nose for avoiding the sort of trouble Greenberg’s piece would have created, were it to be unleashed on the population—and although they like to call themselves journalists, that’s a myth even they don’t really believe anymore. They’re mutts on short leashes.

Dr. Allen Frances (twitter) is the man who, in 1994, headed up the project to write the latest edition of the psychiatric bible, the DSM-IV. This tome defines and labels and describes every official mental disorder in the known universe. The DSM-IV eventually listed 297 of them.

In an April 19, 1994, New York Times piece, “Scientist At Work,” Daniel Goleman called Frances “Perhaps the most powerful psychiatrist in America at the moment…”

Well, sure. If you’re sculpting the entire canon of diagnosable mental disorders for your colleagues, for insurers, for the government, for pharma (who will sell the drugs matched up to the 297 DSM-IV diagnoses), you’re right up there in the pantheon.

But 12 years later, long after the DSM-IV had been put into print, Frances talked to Wired’s Greenberg and said the following:

There is no definition of a mental disorder. It’s bullshit. I mean, you just can’t define it.”

That’s on the order of the designer of the Hindenburg, looking at the burned rubble on the ground, remarking, “Well, I knew there would be a problem.”

That’s much more serious than the president telling the American people, “We sent our combat planes to Libya, but I meant to say Liberia.”

After a suitable pause, Dr. Frances remarked to Greenberg, “These concepts [of distinct mental disorders] are virtually impossible to define precisely with bright lines at the borders.”

Obliquely, Frances might have been referring to the fact that his baby, the DSM-IV, had rearranged earlier definitions of ADHD and bipolar to permit many more diagnoses, leading to a vast acceleration of drug-dosing with highly powerful and toxic compounds.

Finally, at the end of the Wired interview, Frances went off on a quite intriguing foray, praising what amounts to a mass-population placebo effect which would justify the existence of the entire psychiatric profession.

Diagnosis [as spelled out in the DSM-IV] is part of the magic…you know those medieval maps? In the places where they didn’t know what was going on, they wrote ‘Dragons live here’…we have a dragon’s world here. But you wouldn’t want to be without the map.”

Here is the import of Dr. Frances’ words: People need to hope for the healing of their troubles; so even if we’re shooting blanks and pretending to know one kind of mental disorder from another, even if we’re inventing these mental-disorder definitions based on no biological or chemical diagnostic tests—since the tests don’t exist and we’re just juggling lists of behaviors—it’s a good thing, because people will then believe there is hope for them; they’ll believe it because we place a name on their problems…

If I were an editor at one of the big national newspapers, and one my reporters walked in and told me, “The most powerful psychiatrist in America just said the DSM is bullshit but it’s still important,” I think I’d make room on the front page.

If the reporter then added, “This shrink was in charge of creating the DSM-IV,” I’d clear more room above the fold.

If the reporter went on to explain that the whole profession of psychiatry would collapse overnight without the DSM, I’d call for a special section of the paper to be printed.

I’d tell the reporter to get ready to pound on this story day after day for months. I’d tell him to track down all the implications of Dr. Frances’ statements.

I’d open a bottle of champagne the toast the soon-to-be-soaring sales of my newspaper.

And then, of course, the next day I’d be fired.

Because there are powerful multi-billion-dollar interests at stake, and who in his right mind would challenge them?

And as I walked out of my job, I’d see a bevy of blank-eyed pharmaceutical executives marching into the office of the paper’s publisher, ready to read the riot act to him.

But oh well; would I have a candidate for biggest bullshitter in America? Just asking.

And as I chewed my cud and wandered the avenues of the big city, I’d look at all the people and something would seep in: the difference between the delusion called reality, which all these people accept, and the actual state of affairs: the giant con game, the giant shell game that allows the drugs to be sold, the drugs that—each and every one—deliver what the shrinks politely call “adverse effects.”

Look them up sometime, if you have a strong stomach.

Here is a sampling:

Adverse effects of Valproate (given for a bipolar diagnosis) include:

acute, life-threatening, and even fatal liver toxicity;

life-threatening inflammation of the pancreas;

brain damage.

Adverse effects of Lithium (also given for a bipolar diagnosis) include:

intercranial pressure leading to blindness;

peripheral circulatory collapse;

stupor and coma.

Adverse effects of Risperdal (given for “bipolar” and “irritability stemming from autism”) include:

serious impairment of cognitive function;

fainting;

restless muscles in neck or face, tremors (may be indicative of motor brain damage).

In 1986, The International Journal of the Addictions published a most important literature review by Richard Scarnati. It was called “An Outline of Hazardous Side Effects of Ritalin (Methylphenidate)” [v.21(7), pp. 837-841].

Scarnati listed a large number of adverse affects of Ritalin and cited published journal articles which reported each of these symptoms.

For every one of the following (selected and quoted verbatim) Ritalin effects, there is at least one confirming source in the medical literature:

Paranoid delusions
Paranoid psychosis
Hypomanic and manic symptoms, amphetamine-like psychosis
Activation of psychotic symptoms
Toxic psychosis
Visual hallucinations
Auditory hallucinations
Can surpass LSD in producing bizarre experiences
Effects pathological thought processes
Extreme withdrawal
Terrified affect
Started screaming
Aggressiveness
Insomnia
Since Ritalin is considered an amphetamine-type drug, expect amphetamine-like effects
Psychic dependence
High-abuse potential DEA Schedule II Drug
Decreased REM sleep
When used with antidepressants one may see dangerous reactions including hypertension, seizures and hypothermia
Convulsions
Brain damage may be seen with amphetamine abuse.

A recent survey revealed that a high percentage of children diagnosed with bipolar had first received a diagnosis of ADHD. This is informative, because Ritalin and other speed-type drugs are given to kids who are slapped with the ADHD label. Speed, sooner or later, produces a crash. This is easy to call “clinical depression.” Then comes Prozac, Paxil, Zoloft. These drugs can produce temporary highs, followed by more crashes. The psychiatrist notices this up and down pattern—and then comes the diagnosis of bipolar (manic-depression) and new drugs, including Valproate and Lithium.

In the US alone, there are at least 300,000 cases of motor brain damage incurred by people who have been prescribed so-called anti-psychotic drugs (aka “major tranquilizers”). Risperdal is one of the major tranquilizers. (source: Toxic Psychiatry, Dr. Peter Breggin)

This psychiatric drug plague is accelerating across the land.

Where are the mainstream reporters and editors and newspapers and TV anchors who should be breaking this story and mercilessly hammering on it week after week? They are in harness.

Jon Rappoport

The author of two explosive collections, THE MATRIX REVEALED and EXIT FROM THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free emails at www.nomorefakenews.com