Posts Tagged ‘Citizens Commission on human rights’

Hickierie Dickory Doc – McGorry Turns Back the Clock

Monday, May 30th, 2011

Seroxat Sufferers – Stand Up and Be Counted
By Bob Fiddaman
May 30, 2011

Patrick McGorry

McGorry’s Delorean continues on it’s trip back to the future in Australia, it’s new passenger, Prof Ian Hickie.

I say new, Hickie has been around for years.

Judging by an article in today’s Australian Telegraph, there seems to be questions being asked regarding the number of Australian children being prescribed antidepressant medication.

Elissa Doherty and Marianne Betts write:

The number of children aged six and under being prescribed anti-depressants has soared by almost 50 per cent since the federal government pledged to investigate the issue, new figures show.

Thing is, just two meetings have been held since Australian Health Minister, Nicola Roxon, ordered an investigation over three years ago!

In the meantime, McGorry’s Delorean [early intervention program] continues to pick up speed…with government backing!

Ian Hickie

Ian Hickie was the inaugural CEO (2000-2003) of ‘beyondblue: the national depression initiative’, which has very successfully sold depression in Australia, with many millions of dollars of government money. This has worked brilliantly for the drug companies, and beyondblue does not accept pharma funding, so the drug companies get the promotion for free. I’ve previously wrote about beyondblue back in November 2008.

Graham “Biff Tannen” Burrows, whom I wrote about here, is now retired but has played a huge role in promoting psychiatric diagnoses and psychotropic drugs in Australia, particularly in the 1990′s.

It would appear that Burrows has been totally in bed with the pharmaceutical companies. More importantly, he influenced government policy in the 1990′s to focus on depression. Without him, it could be suggested that beyondblue would not have come about nor would McGorry’s meteoric rise a decade or so later.

Beyondblue and Hickie paved the way for EPPIC, a psychiatric service aimed at addressing the needs of older adolescents and young adults with emerging psychotic disorders.

Hickie, it would appear, is the Burrows of the 21st century.

McGorry shot to fame last year when he was appointed Australian of the Year. Hickie and McGorry had already been working together for several years, in fact Hickie is a key player in McGorry’s ‘Headspace’).

Anything they say to the Aussie government seems to be taken at face value, this is something that baffles me. We can all make claims about “fixing” mental disorders because they simply cannot be diagnosed. The way forward for Australians is nipping these disorders in the bud by ‘catching them early.’ I cannot believe the Aussie government could fall for this – what evidence has McGorry supplied to back up these claims?

Whatever they say is usually accepted as gospel, and it is very rare for either of them to be criticised, save for a handful of advocates, a few Australian MP’s and the Citizens Commission on Human Rights [CCHR]

SPHERE

The PDF above is a seemingly egregious example of the conflicts of interests that exist: a whole journal supplement based on the SPHERE project clinical audit. The audit was funded by Bristol-Myers Squibb (see p. S54), the manufacturer of Serzone. The publication of the supplement was funded by beyondblue with Commonwealth [Australian] Government money (see title page).

The audit, which used Hickie’s SPHERE questionnaire, found ridiculously high rates of mental disorders. This was reported in the supplement by Hickie, Davenport, Naismith, & Scott (2001, p. 52) as:

‘Sixty-three per cent of people attending general practice have some evidence of mental disorder (including alcohol or other substance misuse) by self-report or GP’s diagnosis of psychological difficulties.’

63%?

That’s some cash cow huh?

Not surprisingly, if you scroll to the bottom of the PDF you will find: Source: Hickie et al. Educational Health Solutions; 2000

McGorry claimed in a recent interview, “…we are trying to do is provide effective treatment for those young people for what they are presenting with and trying to reduce the risks. There are other effective ways of reducing the risk including cognitive behaviour therapy, the use of omega-3 fatty acids and so on.”

With previous involvement of Hickie and the pharmaceutical industry, I’d really love to believe that McGorry would use CBT and omega-3 fatty acids etc to help kids diagnosed with a mental disorder…before they actually get it!

I am left wondering if the Australian government have done their homework on McGorry & Co or if they just like to throw money into projects without first taking a look at the scientific proof – Has the current Australian Prime Minister, Julia Gillard, ever sought to seek evidence about the chemical imbalance myth? Has she taken a good look at the deaths associated with psychiatric drugs?

Here’s an idea for the Aussie PM, ask for scientific proof of McGorry & Co’s time-travelling prediction vehicle, don’t just take it as gospel that it works.

For the record, and so Patrick McGorry and his cronies totally understand, I was raised a Catholic. I denounced myself as one in later years. McGorry & Co can throw the Scientology tag at me if they wish, they have done it in the past when backed into a corner by CCHR. If that is all they have in their armour then I envisage a future of mind altering drugs being prescribed to Australian children on the basis that they may have an illness rather than they actually have an illness. If parents of those children dare question McGorry & co, prepare yourselves for some mud slinging – you may as well sign yourselves up to the Church of Scientology, you’ll be labelled one regardless…and we all know how psychiatrists, such as McGorry, just love to use labels.

How do I know this? Well, like McGorry & Co, I travelled forward in time…in my Tardis – my DeLorean is at the garage in need of a new flux capacitor.

Fid

http://fiddaman.blogspot.com/2011/05/hickierie-dickory-doc-mcgorry-turns.html

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The Fraudulent Nature of Psychiatric Labels Exposed by Human Rights Group

Monday, April 25th, 2011

There are no genetic tests, no brain scans, blood tests, chemical imbalance tests or X-rays that can scientifically/medically prove that any psychiatric label is a real medical condition.

Vancouver, British Columbia — (SBWIRE) — 04/25/2011 — A new must-see video produced by the Citizens Commission on Human Rights International graphically demonstrates the fraudulent nature of psychiatry’s labels.

In real life, 20 million children are now wearing these labels that are based solely on a checklist of behaviors. There are no brain scans, x-rays, genetic or blood tests that can prove the scientific validity of any of the psychiatric labels, yet these children are prescribed dangerous and life-threatening psychiatric drugs based on nothing more than the invented label.

Child drugging is a $4.8 billion-a-year industry.

The psychiatric/pharmaceutical industry spends billions of dollars a year in order to convince the public, legislators and the press that these labels such as Bi-Polar Disorder, Depression, (ADD/ADHD), Post Traumatic Stress Disorder, etc., are medical diseases on par with verifiable medical conditions such as cancer, diabetes and heart disease. This is simply a way to maintain their hold on a $84 billion dollar-a-year psychiatric drug industry that is based on marketing and not science.

Brian Beaumont, president of the Vancouver chapter of the Citizens Commission on Human Rights (CCHR) said, “Unlike real medical disease, there are no scientific tests to verify the medical existence of any psychiatric disorder. Falsely labeling children is fraud and drugging these children is child abuse”.

Despite decades of trying to prove mental disorders are biological brain conditions, due to chemical imbalances or genetic factors, psychiatry has failed to prove even one of their hundreds of so-called mental disorders is due to a faulty or “chemically imbalanced” brain”.

http://www.sbwire.com/press-releases/sbwire-89685.htm

To find out more about psychiatric diagnosing, labels and drugs, click here: http://www.cchrint.org/psychiatric-disorders/

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Psychiatrist Patrick McGorry Ticked Off CCHR’s Busted Him Over Bogus “Early Intervention” Claims

Thursday, April 21st, 2011

Psychiatrist Patrick McGorry promotes a highly dangerous and outrageous agenda of pre-diagnosing youth as mentally ill "before" they develop it...

Seroxat Sufferers – April 21, 2011

by Bobby Fiddaman

I had to laugh at the article from the Herald written last August.

It would appear that Australian psychiatrist Patrick McGorry [originally an Irish born lad] doesn’t like it when he is brought to task regarding his early intervention claims [He can predict if a child can get a mental disorder in later years you know]

The article,  written by Brigid O’Connell, lays claim that McGorry has become the target by the Church of Scientology after he and other psychiatrists spoke out against them.

I think you will find that it’s the other way around.

The Citizens Commission on Human Rights [CCHR] have, for a long time, been on McGorry’s back. Where McGorry gets confused [bless him] is that CCHR is not the Church of Scientology. Okay, CCHR was founded by the Church [and actually also a psychiatrist Thomas Szasz, who no doubt wouldn't agree with your "early intervention" drugging kids fad either] but they are funded by Tom, Dick and Harry…that is, by anyone concerned enough about human rights.

CCHR have requested documents under the Freedom of Information Act. Documents that may or may not show McGorry’s links to the pharmaceutical industry. We are not talking about a free dinner here, we are talking millions of Aussie dollars.

You see, McGorry has devised a program whereby it could be…um…guessed through early intervention if children would develop a mental disorder in later years. Your modern day DeLorean time machine if you will.

One would imagine that such a test would involve some sort of brain scanning machine or maybe a series of blood tests. Nope… just form filling or rather box-ticking. That’s all the info the early intervention program needs to diagnose [stigmatise] a child…or rather “predict” if a child will fall foul to a mental disorder. Hey, and McGorry and friends know exactly how to treat this invisible futuristic illness too.

I find it odd that McGorry would cry victim, even more so that he would claim to be the target of “harassment.” Would he do the same if Joe Bloggs requested information under the Freedom of Information Act or is he just pissed at CCHR? If the Catholic Church were to request such documents would McGorry & Co scream that they were being victimised?

For the record Paddy [McGorry], I’m not a great fan of yours either. I’d also like to see if you are funded by the industry and would ideally love to take a ride in your Delorean to predict now if I will get an ingrowing toenail when I’m 55. “Please Massa, show me the boxes to tick. I promise to be a gooooood patient”

Oh, I’m not a Scientologist either but have won two human rights awards from CCHR. Geez, they must have “brainwashed” me [which, by the way Paddy, only your drugs can do]…can your early intervention program undo what they have done to my brain? Can you give me some drugs please Paddy?

Come on Paddy, be a good little psychiatrist and show the world that you have nothing to hide…unless of course you have something to hide? Show the Aussie government the $3.5 billion “investment” plan for its kids you want to rip off the taxpayers isn’t gonna be used to put them on antipsychotics that those drug companies which probably fund you are going to benefit from. Is this really why you feel harassed – you may not get your booty?

The only way people can seek the truth is by going through proper channels, namely by using the Freedom of Information Act. That’s their given right, Paddy! Everyone has a right to use this tool be they Scientologists, a human rights movement, someone who claims to be from the planet Zog or someone who has delusions that Shania Twain will one day mattress dance with them.

Oh by the way, I walk under ladders as I’m not very superstitious – if I were to avoid walking under ladders I’m sure your profession would label me with some disorder, have me drugged to the eyeballs, restrained and injected with experimental drugs. Maybe you can tell me if I will walk under ladders in future years?

Face it, your crystal ball is no more effective than a fortune teller at the end of a seaside pier. At least she has the signs outside telling customers that she is paid for her crystal ball gazing.

It never ceases to amaze me that when psychiatrists are backed into a corner they scream victim. When their patients are backed into a corner, restrained, injected and/or force-fed psychiatric drugs they have no choice but to take it on the chin.

Your Delorean needs a new flux capacitator Paddy. CCHR are coming to getcha…and there are many who support their work.

Bob Fiddaman
Shania Twain fan.

http://fiddaman.blogspot.com/2011/04/psychiatrist-patrick-mcgorry-slams-his.html

Read more about Patrick McGorry here: Prison Planet -Pharma Backed Australian of the Year Psychiatrist Wants Millions in Government Funding for Brave New World of Pre-Drugging Kids

http://www.prisonplanet.com/pharma-backed-australian-of-the-year-psychiatrist-wants-millions-in-government-funding-for-brave-new-world-of-%E2%80%9Cpre-drugging%E2%80%9D-kids.html

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FDA Advisory Panel Recommends Electroshock Machine Too Risky For Reclassification to Less Dangerous Device

Monday, January 31st, 2011
A panel of the U.S. Food and Drug Administration (FDA) recommended Friday that devices used to deliver ECT, or psychiatric shock treatment, remain in the most high-risk category (Class III), reserved for the most dangerous medical devices.

January 31, 2011

by CCHR International— The Neurological Devices Advisory Panel of the U.S. Food and Drug Administration (F.D.A.), recommended Friday that devices used to deliver shock treatment, also known as electroconvulsive therapy (ECT) remain in the most high-risk category (Class III), reserved for the most dangerous medical devices and not be downgraded to a lower risk category.  In so doing, it recommended that the companies which manufacture ECT devices be required to prove that ECT is both effective and safe in order to remain in use.

ECT has long been known to cause serious harm to patients, including extremely severe and permanent memory loss, inability to learn and remember new events, depression, suicide, cardiovascular complications, prolonged and dangerous seizures and even death.

Patients who have undergone ECT felt vindicated by the decision, saying the ECT device is dangerous and causes irreparable harm.  The chairman of the advisory panel, Dr. Thomas G. Brott, a Professor of Neurosciences, at the Mayo Clinic expressed concern about 100,000 people being given ECT each year in the U.S., yet psychiatrists had not bothered to conduct MRI scans before and after the procedure to monitor potential brain damage.

Ms. Jan Eastgate, President of the Citizens Commission on Human Rights (CCHR), a psychiatric watchdog, spoke at the Hearing and was critical of the ECT device manufacturers, Mecta and Somatics, Inc. for their failure to conduct safety studies and submit a Pre-Marketing Application (PMA), while making more than $30 million from sales of the machine over the past 3 decades.  She said psychiatrists claiming that a PMA would be “too expensive” had put profit above patient safety— With ECT costing between $1,000 and $2,500 a treatment, psychiatrists had made more than $28 billion during the same period.

The hearings were prompted by a GAO investigation in January 2009 resulting in a report stating the FDA must examine all devices which had remained for a substantial time in Class III without critical evaluation of safety and effectiveness. The GAO said the FDA should take steps to ensure that high-risk device types are approved through the most stringent review process reserved for new machines coming on to the market which may be potentially dangerous.

The FDA Office of Medical Device Evaluation thereafter called for hearings before a panel of experts to advise the FDA whether shock devices could be downgraded to Class II – and therefore require little review – or remain in the highest risk category with a mandated approval process with stringent clinical trials. The FDA Advisory Panel agreed that this device was sufficiently dangerous to require that it remain in Class III.  It is up to the FDA whether to act on the recommendations of the panel.

Ms. Eastgate said the decision is the first step towards getting needed greater protections for patients but said there were still considerable concerns about the F.D.A.’s handling of the safety and efficacy issues concerning ECT.  She said there are potential conflicts of interest with psychiatrists helping write the F.D.A.’s Executive Summary on ECT and advising the agency about the procedure.

Watch video: Electroshock—It’s Not Treament, It’s Torture

here:  http://www.youtube.com/watch?v=QDR3cD8_kck

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Parents Warn of Possible Psychiatric Drug Dangers

Saturday, November 27th, 2010

The Post & Courier

by Glen Smith

Matthew Steubing committed suicide by jumping from the Silas Pearman Bridge in Charleston on July 18, 2003. He was 18.Matthew Steubing committed suicide by jumping from the Silas Pearman Bridge in Charleston on July 18, 2003. He was 18.

Darkness hung over Charleston Harbor as Matthew Steubing parked his Ford pickup truck on the aging bridge and left a note on the seat beside his Bible. He put on a life jacket and began to climb — up, up, into the span’s superstructure.

Then, he jumped.

His parents were waiting for Matthew to arrive home in Winchester, Va., when they received the news on July 18, 2003. Their 18-year-old son plunged more than 160 feet from the Silas Pearman Bridge before slamming into the Cooper River. He was gone.

“Our world blew apart,” his mother, Celeste Steubing, said. “We couldn’t imagine this happening because this wasn’t Matthew. … It made no sense.”

Matthew, the youngest of six children, had been a vibrant kid, happy and full of life. But after a rough patch in his senior year of high school left him feeling down, a psychologist suggested he would benefit from the antidepressant drug Lexapro. He soon became withdrawn and anxious, his parents recalled during a recent visit to Charleston.

Matthew committed suicide just nine weeks after starting on the drug. Only later did his family learn that antidepressants carry a heightened risk of suicide in children, the Steubings said.

The Steubings have made it their mission to warn other parents about the hidden dangers of psychiatric drugs. To that end, Celeste Steubing was featured in the recently released documentary, “Dead Wrong,” produced by the Los Angeles-based Citizens Commission on Human Rights.

The 90-minute film profiles Matthew’s story and documents Celeste Steubing’s travels to speak with doctors, health experts, drug counselors and other mothers with painful tales of loss associated with psychiatric drugs.

Forest Laboratories, makers of Lexapro, would not comment on Matthew Steubing’s case but defended the drug’s safety in a prepared statement. The company stated that antidepressants such as Lexapro have been associated with a substantial reduction in the suicide rate in the United States.

“Forest has tremendous sympathy for any family dealing with the suicide of a loved one, and Forest understands that family members dealing with such a tragedy often are looking for answers,” the statement read. “However, Lexapro is a safe and effective medication for the treatment of major depressive disorder in patients as young as 12, when used according to the FDA-approved package insert.”

Celeste Steubing and her husband, Daniel, said Matthew had never been suicidal before going on the drug, which was prescribed by a doctor to correct a perceived chemical imbalance.

The couple said they would not have given Matthew the Lexapro had they known it carried a risk of increased suicidal thinking and behavior in children and young adults. The drug’s label now carries that “black box” warning.

Matthew quickly went downhill on the drug, the Steubings said. He had trouble sleeping, lost weight and seemed agitated and out of sorts. Normally outgoing, he became distant and isolated, they said.

“He was like a caged cat,” his father said. “We couldn’t understand what was happening to him.”

After balking at a long- anticipated beach trip with friends, Matthew opted to travel to Charleston in July 2003 to visit his older brother Eric, who was attending college here. He stayed for 10 days before bidding his brother goodbye on July 18, 2003. Matthew called his mother that day to report his progress heading home. His last call indicated he had just passed through Roanoke, Va.

In reality, Matthew was still in the Charleston area, apparently planning his own death. In the note he left behind, he indicated that he wore a life vest so his family wouldn’t have to look for his body and worry about where he was.

After reading an article about a possible link between antidepressants and suicide, the Steubings started digging and doing research of their own. The more they learned, the angrier they got.

They went on to testify at a 2004 Food and Drug Administration hearing in Washington, D.C., that led to the warning labels. Telling Matthew’s story still brings pain and tears, but they continue to speak out.

“It’s important so that other parents don’t have to go through the heartache and anguish we have,” Celeste Steubing said. “So that other parents don’t have to miss their children for the rest of their lives like we do.”

http://www.postandcourier.com/news/2010/nov/27/parents-warning-others/

To view the documentary, Dead Wrong: How Psychiatric Drugs Can Kill Your Child,  click here http://www.cchr.org/take-action/parents/message-to-parents.html

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1 million misdiagnosed ADHD children for $80B drug industry

Saturday, October 30th, 2010

Examiner.com
By Deborah Dupre
October 30, 2010

Two new studies published suggest something wrong with the way ADHD is diagnosed in young children in the US, confirming the need for the public to utilize Citizens Commission on Human Rights International resources for injury prevention.

One or the new studies found nearly 1 million children potentially misdiagnosed just because of being youngest in their kindergarten year, with the class youngest twice likely to be medicated with stimulant medication. The other study confirmed that whether children were born just before or just after the kindergarten cutoff date significantly affected chances of being diagnosed ADHD.

20 million children are taking psychiatric drugs according to the mental health watchdog, Citizens Commission on Human Rights International (CCHRI).

CCHR works shoulder-to-shoulder with like-minded groups and individuals who share a common purpose to restore basic inalienable human rights to the field of mental health. These rights include, but are not limited to, full informed consent regarding risks of treatments and all available medical alternatives, and the right to refuse any treatment considered harmful.

Psychiatric disorders fuels an 80 billion dollar industry, highlighted CCHTI’s new documentary online, THE STAMP: Psychiatric Disorders Fuel $80 Billion Drug Industry.

Most authors of the “official” Diagnostic Manual that sets criteria for mental “diseases” have ties to the drug industries.”

“The psychiatric/pharmaceutical industry spends billions of dollars a year to convince the public, legislators and the press that psychiatric disorders such as Bi-Polar Disorder, Depression, Attention Deficit Disorder (ADD/ADHD), Post Traumatic Stress Disorder, etc., are medical diseases on par with verifiable medical conditions such as cancer, diabetes and heart disease. Yet unlike real medical disease, there are no scientific tests to verify the medical existence of any psychiatric disorder. To counter this obvious flaw in their push to medicalize behaviors, the psychiatric industry will claim that there are certain medical conditions that do not have a verifiable test so this is why there isn’t one for “mental illness.” This is frankly a lame argument; Whereas there may be rare medical conditions that do not have a verifiable medical test, there are virtually no psychiatric disorders that can be verified medically as a physical abnormality/disease. Not one.” (CCHR)

Parents, legislators and the general public are not being given documented risks of drugs prescribed to children. CCHRI provides an easy to use search engine with complete information including warnings, studies, and adverse reactions to psychiatric drugs at www.cchrint.org/psychdrugdangers/.

No More ADHD

Dr. Mary Ann Block, Medical director of the Block Center and associated with CCHRI is an outspoken critic of children being diagnosed ADHD and put on drugs documented to cause tics, stunted growth, heart attack, stroke and sudden death.

Dr. Block describes how parents are being misinformed about the medical legitimacy of ADHD and the dangers of the drugs being prescribed to treat children. She encourages parents to have their child given a full medical examination to find underlying medical problems that are being misdiagnosed as a mental disorder.

The Citizens Commission on Human Rights (CCHR) is a mental health watchdog and non-profit organization. It has been responsible for more than 150 laws protecting individuals from abusive or coercive practices committed under the guise of mental health.

CCHR’s Board of Advisers, called Commissioners, include doctors, scientists, psychologists, lawyers, legislators, educators, business professionals, artists and civil and human rights representatives.

Co-founder of CCHR, Dr. Thomas Szasz is a Professor of Psychiatry Emeritus at the State University of New York, Adjunct Scholar at Cato Institute and Lifetime Fellow of the American Psychiatric Association. Considered by many scholars and academics to be psychiatry’s most authoritative critic, Szasz has authored over 35 books on the subject, the first being The Myth of Mental Illness, a book that rocked the foundations of psychiatry upon its release more than 50 years ago.

Photo: CCHR International

Watch the full CCHR documentary, THE STAMP: Psychiatric Disorders Fuel $80 Billion Drug Industry, here.

Read the entire article here:  http://www.examiner.com/human-rights-in-national/1m-misdiagnosed-adhd-children-for-80b-drug-industry

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Psychiatric Meds 101: A Surprising Discovery – Your Own Personal Hell

Tuesday, July 20th, 2010

Mouse over image and click to see next slide. To copy/post slideshow use the embed code at bottom of page.

By Shane “The People’s Chemist” Ellison
Author, Over-The-Counter Natural Cures

I may be a perfect candidate for psychiatry.

I ask questions with period marks to shorten conversations. I avoid eye contact with strangers in fear (maybe it’s anxiety) that I might learn too much about them. I secretly think that Metallica would be making better music if they went back to bludgeoning themselves with party drugs and alcohol, instead of “therapy.” I’m trying to master the Law of Un-attraction to shield myself from a “real job,” small homes and junky cars.  And, I’m constantly giving my children advice, only to give it to myself.

Psychiatry, can your drugs help me?

Perhaps these questions are what motivated me to pursue a career as a drug design chemist, winning multiple awards for my work. Nothing gets me more excited than drugs and how they affect the body (except my wife’s abs). I’ve studied their molecular anatomy, risked life and limb to mix and match explosive chemicals in a round bottom flask, and even sold my soul to Big Pharma in exchange for a lab bench and chemical hood.

During this time, I’ve made some surprising discoveries about psychiatric meds, which include antidepressants, antipsychotics, stimulants, and anti-anxiety drugs. Understanding what I’ve learned will protect you from the flood of side effects that are now being discovered at breakneck speeds, courtesy of the myriad of patients being prescribed psychiatric drugs in the name of mental health.

Your Own Personal Hell

Antidepressants strive to increase the levels of a “coping” molecule known as serotonin in the brain. It supposedly helps us find happiness when it’s covered in an avalanche of nastiness. But, it’s never been proven. Still, the drugs attempt to boost serotonin by “selectively” stopping the “reuptake” among brain cells. This is where the whole SSRI acronym came from—“selective serotonin reuptake inhibitor.” It’s a slick name, but a stupid idea. Nothing is selective in the body.

While trying to block the reuptake of serotonin, antidepressants can also prevent its release and that of another brain compound known as dopamine. The areas of the brain responsible for release and reuptake of these neurotransmitters are so damn similar (after all, they work on the same molecule) that an antidepressant drug isn’t smart enough to understand which one it is supposed to work on. So it does what any dumb drug would do, it blocks both. That’s why users usually carry a glassy stare in their eye. Fully under the psychiatric spell, they’ve tuned out.

Deep sadness, fear, anger and aggression can set in over time. By removing serotonin and dopamine from the brain, long-term antidepressant users can’t find or feel happiness. Instead, they may become buried in the avalanche of nastiness. And if you can’t find or feel happiness in life, what’s the point? What’s going to stop you from snapping your own neck or spraying bullets on your classmates? Not much when you live in your own personal antidepressant hell.

Think this is all opinion?

According to the FDA, antidepressants can cause suicidal thoughts and behavior, worsening depression, anxiety, panic attacks, insomnia, irritability, hostility, impulsivity, aggression, psychotic episodes and violence.  Some even cause homicidal ideation according to the manufacturers. Many long-term antidepressant users will tell you they no longer feel normal emotions—they’re numb, like zombies.

But the side effects of these drugs aren’t limited to hijacking your feelings and emotional state, causing violent and psychotic states. Physical side effects occur too and include abnormal bleeding, birth defects, heart attack, seizures and sudden death. Over one hundred and seventy drug regulatory warnings and studies have been issued on antidepressants, to sound the alarm on these side effects.

For Elephant Use Only

Psychiatrists prescribe antipsychotic meds such as Zyprexa and Seroquel, for anything from schizophrenia, bipolar disorder, delusional disorder, psychotic depression, autism or anything else they can think of, even “pervasive developmental disorder,” which is perfect for boosting sales because it targets children who suffer from irritability, aggression, and agitation. It’s a shame ‘cause these drugs are good for nothing but sedating irate elephants, not curing psychiatric disease.

According to a study published in Psychological Medicine, antipsychotic drugs cause brains to shrink – they lessen brain matter and volume. Originally designed for those deemed “schizophrenic,” the drug companies came up with a brilliant marketing campaign to sell these drugs to a much wider market—unsatisfied antidepressant users. You’ve probably seen the ads—if your “depression medication” isn’t working, then don’t blame the drug; you may just have bipolar disorder!

Once swallowed, antipsychotics sail through the blood stream where they’re carried to the brain. Like a giant oil spill, antipsychotics cover the brain in a medicinal slick, where brain wave transmission is blocked. Users become devoid of normal brain activity. Motivation, drive and feelings of reward are shunted. If psychiatry considers this a “treatment,” they’re the crazy ones.

If you’ve ever seen someone who has suffered from the “spill” courtesy of following doctors orders, you can’t mistake one of the most common side effects, it’s called Akathisia. Involuntary movements, tics, jerks in the face and the entire body can become permanent side effects for antipsychotic users.

Antipsychotics also cause obesity, diabetes, stroke, cardiac events, respiratory problems, delusional thinking and psychosis. Drug regulators from the U.S., Canada, United Kingdom, Ireland, Australia, New Zealand and South Africa warn that they can also lead to death. I wouldn’t be surprised if psychiatrists considered this a cure…

Use This to Jump The Grand Canyon

If you’re going to attempt to jump your scooter over the Grand Canyon, or ride your snowboard off Kilimanjaro, stimulants are great. They flood the brain with dopamine and trigger an inhuman surge of adrenaline, responsible for making you believe life is grand, despite eminent death. Outside of that, you’re either a speed freak, a college student trying to learn an entire semester of Biology 101 in 4 hours, or a fifth grader “following doctor’s orders.”

Top stimulants being prescribed today are nothing more than a mix of amphetamines packaged into trade names like Adderall, Dexedrine and Ritalin.  Street thugs sell it as meth, poor man’s cocaine, crystal, ice, glass and speed. It’s no wonder kids are now abusing Ritalin, Adderall and these drugs more than street drugs, they’re cheaper to get and they’re “legal,” hence the term kiddie cocaine.

Even the U.S. Drug Enforcement Administration (DEA) categorizes Ritalin in the Schedule ll category, meaning a high potential for abuse—just like cocaine and morphine. All of them have the same effects regardless of how they’re named: Central nervous system overload leading to heart attack and/or heart failure. And kids are dropping faster than Meth Heads at Raves…

I’m not exaggerating.

Eleven international drug regulatory agencies and our own FDA has issued warnings that stimulants like Ritalin cause addiction, depression, insomnia, drug dependence, mania, psychosis, heart problems, stroke and sudden death.

 Bash Your Head in with Anti-Anxiety Drugs

If you’re not man enough for a drug that could sedate an elephant like antipsychotics, then psychiatrists will prescribe anti-anxiety meds, particularly benzodiazepines. Choosing between the two is akin to deciding whether or not you should be hit in the head with an aluminum bat or a wooden one; anti-anxiety meds being the latter.

Discovered in the stinky chemistry labs of Hoffman La Roche in 1955, anti-anxiety meds aim to trigger sleep receptors in the brain, just slightly. So, rather than being riddled with anxiety, you are put to sleep, halfway. It’s “treatment,” and psychiatrists have been “practicing it for decades.” But, it has yet to work, because drugging your problems away is more dangerous than anxiety. The use of anti-anxiety meds is coupled with a host of nasty side effects such as seizures, aggression and violence once the drug wears off. Hallucinations, delusional thinking, confusion, abnormal behavior, hostility, agitation, irritability, depression and suicidal thinking are all possible outcomes according to Big Pharma’s heavily guarded research papers.

Getting off the drugs could be harder than abandoning a heroin addiction. Some have described withdrawal from “benzos” being akin to pulling hundreds of fish hooks out of their skin, without anesthesia. If you doubt their addictive nature, go to Google search and type in a few of the leading anti-anxiety drugs like Klonopin or Xanax and here is what you’ll find:

“Klonopin withdrawal” 1,860,000 results

“Xanax withdrawal” 1,980,000 results

Exposing Psychiatry: How to Get The Truth

In total, the side effects of psychiatric meds spread far and wide. And most are hidden from patients and doctors alike. Fortunately, Citizens Commission on Human Rights has solved this problem with a state-of-the-art database that allows people to search through the adverse reaction reports sent to the FDA on psychiatric drugs. It also provides international drug regulatory agency warnings and studies published on the side effects of the drugs.

So, can psychiatry help me? No. And that’s surprising because psychiatric meds are some of the biggest selling drugs, poised to seal the hopes and dreams of millions.  Regardless of what mental state I might be in (or anyone else for that matter), there is not a single drug that cures, treats or solves the perceived problems of mental health.

While people can suffer miserably from emotional or mental duress that can hinder their lifestyle, the pseudo-science of psychiatry has yet to solve any of these problems, and in fact only contributes to poor health as seen by the wide array of side effects. Marketing campaigns and ghostwritten medical journals are designed to obscure these facts. But the psychiatric drug side effect database courtesy of CCHR ensures that all patients have access to the truth, to the documented facts, which could save their life or that of a loved one.

 About the Author

Shane Ellison holds a masters degree in organic chemistry and is the author of Over-The-Counter Natural Cures.  An award winning chemist, he has been quoted by USA Today, Shape, Woman’s World, as well as Women’s Health and appeared on Fox and NBC as a natural medicine advocate.  Sample his book free at www.thepeopleschemist.com

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SSRIs Render Unfriendly Skies—FOIA documents reveal what FAA failed to consider in allowing pilots on antidepressants to fly

Wednesday, July 14th, 2010

Scoop Independent News
By Evelyn Pringle
July 14, 2010

The SSRI antidepressant makers are desperate to find new customers, so they recently have been focusing on capturing groups for which the drugs were usually considered off limits. The latest marketing coup managed to open up sales to roughly 614,000 American pilots.

Under a new policy announced on April 5, 2010, pilots diagnosed with depression can seek permission from the Federal Aviation Administration to take one of four SSRIs, including Eli Lilly’s Prozac, Pfizer’s Zoloft, and Forest Laboratories’ Celexa and Lexapro.

“The FAA should reverse its ruling before it’s too late and hundreds of lives are lost when a pilot becomes impulsive, suicidal or violent–or just loses his sharpness–under the influence of antidepressant medication,” said SSRI expert, Dr Peter Breggin, in an April 19, 2010 Huffington Post commentary.

The Citizens Commission on Human Rights is also calling on the FAA to rethink allowing pilots to take SSRI in light of a new report issued last month by the National Transportation Safety Board, on a February 1, 2008 plane crash in North Carolina, by a crazy acting pilot on Zoloft, that killed all six persons on board

The report said the pilot failed to maintain control of the plane during instrument flying conditions and “deliberately descended below the minimum descent altitude.” The plane stalled and crashed while circling after an aborted landing.

“Review of the cockpit voice recorder (CVR) audio revealed that the pilot had displayed some non-professional behavior before initiating the approach,” the NTSB reported.

The CVR recorded the pilot singing: “Save my life I’m going down for the last time,” before beginning a commentary in which he told passengers: “If anybody back there believes in the good Lord, I believe now would be a good time to hit your knees.”

A review of medical records documented that “from December 4, 2006 through December 31, 2007, the pilot had filled 6 prescriptions for 30 tablets of 50 mg sertraline (Zoloft),” the report said.

The records indicated that he had been treated previously with two other antidepressant medications for “anxiety and depression” and a history of “impatience” and “compulsiveness,” the NTSB noted.

An investigation of another plane crash, resulting in two fatalities in Kingsport, Tennessee, in August 2003, found Zoloft in the blood and liver of a private flight instructor, according to an accident report by the NTSB.

In the policy statement published in the Federal Register, the FAA seems to justify the use of these drugs via the fully debunked “chemical imbalance in the brain” theory when writing: “All these medications are SSRIs, antidepressants that help restore the balance of serotonin, a naturally occurring chemical substance found in the brain.”

“Increasingly accepted and prevalently used, these four antidepressants may be used safely in appropriate cases with proper oversight and have fewer side effects than previous generations of antidepressants,” the FAA wrote, with no citation to any scientific paper to back up this assertion.

In fact, the current labels on SSRIs warn that “anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, and mania, have been reported in adult and pediatric patients treated for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric.”

“Even when not severe, these reactions impair judgment and increase the likelihood of accidents and violence,” according to Dr Breggin.

CCHR has set up a great website with a one-of-a-kind search engine that allows the public and officials to access the database on side effects reported to the FDA on SSRIs, and every other psychiatric drug. The site also has a search engine to access all the International warnings and studies on psychiatric drugs which have been summarized so they are easy to understand, even to a lay person.

Input Only From the Choir

On April 6, 2010, Bob Fiddaman, author of the long-running popular website and blog, “Seroxat Sufferers,” sent a request to the FAA, under the Freedom of Information Act, seeking information on the change in policy.

In the Federal Register, the FAA claims it came to its decision after “careful consideration.” However, in the 58 pages of documents sent to Fiddaman on June 9, 2010 (and kindly shared with this author), there is no mention of consultations with any of the prominent SSRI experts who may have offered a contrary view. Like Peter Breggin for instance.

The FAA’s response to Fiddaman shows the agency has been discussing the policy change since at least 2008. In response to a request for “minutes of meetings where the change in the policy was on the agenda,” as well as a list of “members present and a declaration of interests of each of the members,” the FAA sent a copy of a July 18, 2008, Memorandum, with a summary from one consultants meeting. Three outside experts attended but there were no declarations of interests, or lack thereof, by anyone at the meeting.

The summary noted that the consultants “unanimously agreed that the concept of allowing certain airmen taking antidepressant medication was reasonable and safe.” But the “unanimous consensus” was that only Prozac and Zoloft “were appropriate medications due to the longevity of their use and overall safety.”

“They also felt that only these two should be considered initially, and no other medications considered at this time,” the summary reported.

In responding to the question of whether the new policy would apply to Air Traffic Controllers, the FAA said the “new policy does not presently apply to Air Traffic Control Specialist (ATCS) because the administrative details of the monitoring and follow-up of these employees are yet to be determined. The plan is that ATCSs will eventually be included in a program of this type.”

In response to a request for any information “given to FAA from outside parties that relate to the FAA’S recent change in policy regarding pilots on antidepressant medication,” the FAA sent copies of documents received from the Aerospace Medical Association, the Airline Pilots Association Aeromedical Office, the International Airline Pilots Association, and the United States Army.

“In developing the new policy, the FAA also utilized a variety of medical research literature available in the public domain,” the response said. “We used internet sites such as, but not limited to: The National Library of Medicine PubMed site and the FDA Medwatch.”

The documents Fiddaman received show consideration of a 2003 study of aviation accidents that found SSRIs in 61 pilot fatalities between 1990-2001, in which the psychological condition and/or the drug use was determined to be the cause, or a factor in 16 of the accidents, or 31%.

However, there was no mention of a later November 2006 study titled, “Pilot Medical History and Medications Found in Post Mortem Specimens for Aviation Accidents,” led by Dennis Canfield, from the FAA’s Civil Aerospace Medical Institute, in the “Aviation, Space, and Environmental Medicine” journal.

For this study, toxicological evaluations were performed on 4,143 pilots involved in fatal aviation accidents during the period between January 1, 1993, through December 31, 2003, to identify all pilots found positive for medications used to treat cardiovascular, psychological, or neurological conditions.

The evaluations found one-hundred dead pilots with SSRIs in their systems including forty with Prozac, twenty-six with Zoloft, twenty-one with Paxil, and thirteen with Celexa.

Less than a month after the new policy was announced, in “Aviation International News,” on May 1, 2010, Matt Thurber reported that in a review of 127 accidents in the NTSB database since 1991, containing the word “antidepressant,” only three were nonfatal.

“In 124 of those accidents, 211 people were killed,” Thurber said. “In accident after accident, antidepressants … were found in the tissues of dead pilots, and the pilots had falsified their medical certificate applications to show that they had never been treated for psychiatric problems.”

Read the rest of this article here:  http://www.scoop.co.nz/stories/HL1007/S00116.htm

Read FOIA documents here: http://fiddaman.blogspot.com/p/faa-respond-to-freedom-of-information.html

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New Dawn Magazine—The Brave New World of Pre-Drugging Kids:Patrick McGorry & Psychosis Risk Syndrome by Jan Eastgate

Thursday, July 8th, 2010

New Dawn
By Jan Eastgate
July 8, 2010

Imagine being a parent taking your 10-year-old daughter to the doctor where she gasps for air and suddenly dies in your arms. You are informed afterwards that a toxic dose of prescribed medication caused her death.

Imagine leaving your house to have lunch with friends, while your husband and 11-year-old daughter are happily cuddled together watching your daughter’s favourite TV show Animal Planet. You return home hours later, walk upstairs to her bedroom and find her hanging from the valence of her bed.

Imagine your teenage son is prescribed a medicine because a teacher said he needs it to curb his disruptive behaviour. Months later he is diagnosed with severe diabetes – a known but covered up side effect by the makers of the medicine. He dies shortly afterwards from complications.

These are not isolated incidents. They are representative of those thousands of children and adolescents who died while taking prescribed psychotropic (mind-altering) drugs in the United States. In the above cases, the drugs were prescribed to treat anxiety experienced while sitting for exams or for so-called “Attention Deficit Hyperactivity Disorder” (ADHD), the symptoms of which include fidgeting, losing your pencils, not sitting still, running about or excessively climbing, and butting into other’s conversations.

Australian Child Deaths

An estimated 1,900 Australians under the age of 19 have died while on antidepressants and antipsychotics. More than 30,700 under 18-year-olds were prescribed antidepressants in 2007-2008, including 550 aged 5 and under. Side effects include hallucinations, hostility, psychosis and suicide.

During the same period, more than 9,300 children under 18 – some as young as one – were prescribed antipsychotics, costing the government $3.4 million. Of the 477 deaths reported to the Australian Therapeutic Goods Administration (TGA) linked to antipsychotics, 15 were for ages 0 to 19, including intrauterine deaths. Experts estimate only 1 percent of Adverse Drug Reactions (ADRs) are reported to the TGA, so deaths could be as high as 1,500.

Common side effects of antipsychotics include excessive weight gain, life-threatening diabetes, and an irreversible neurological effect called Tardive Dyskinesia that manifests in uncontrollable twitching of the muscles and extremities and tongue movements. Another adverse effect, Neuroleptic malignant syndrome (NMS) can cause sudden death.1 Statistics the Citizens Commission on Human Rights obtained from the TGA in 2009 revealed 14 incidents of 10 to 19 year olds experiencing NMS were reported to it.

The psychiatric drug abuse of young Australians prompted one Western Australian MP recently to call for a national inquiry into the use of psychotropic drugs in children. To date, the federal government has yet to act.

Instead, it has potentially exacerbated the situation, handing over more than one hundred million taxpayer dollars to Patrick McGorry, Professor of Youth Mental Health at the University of Melbourne, Executive Director of ORYGEN Research Centre, and founder of the youth mental health centre chain, headspace.

Read entire article: http://www.newdawnmagazine.com/articles/the-brave-new-world-of-pre-drugging-kids-patrick-mcgorry-psychosis-risk-syndrome

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Prescription Pill-Popping By Far a Leading Killer as Florida’s Drug Deaths Spike 20%

Thursday, July 1st, 2010

FlaglerLive.Com
July 1, 2010

Oxycodone, the addictive prescription pain-killer also known by its Purdue Pharma brand name OxyContin, directly caused more deaths in Florida in 2009 than cocaine, heroin and morphine combined. Prescription drugs as a whole are killing far more Floridians than illegal drugs, with some 8,600 deaths last year involving at least one prescription drug, according to an annual report released today by the Florida Medical Examiners Commission.

That’s 5 percent of all deaths in Florida in 2009, when 171,300 people died in the state.

The number of people killed by prescription drugs is a significant 20 percent increase over last year’s 6,200 deaths attributed to overdoses. Much of the increase is due to a spike in oxycodone addiction. The increase in prescription-drug addiction continues a trend that began in Florida 10 years ago, when prescription drugs overtook illegal drugs as leading causes of drug-related deaths.

Alcohol is also included in the examiners’ analysis, and it leads the way of all drug-related deaths, with 4,046.

The annual report is a stark look at the effects of legalized drug addiction and over-prescription of drugs, both of which affect a far larger segment of the population than recreational or illegal narcotics.

For the first time in 2009, the commission tracked deaths by region. In Flagler County’s district, which includes St. Johns and Putnam counties, 22 deaths were attributed to oxycodone (the fourth lowest number in the state’s 23 districts), with 13 of those deaths directly attributed to the drug, and nine cited as being present among other drugs that contributed to death.

Hydrocodone claimed 16 lives in the district. Cocaine contributed to 19 deaths in the Flagler district, though only four cases were directly attributed to the drug. In 15 cases, cocaine was present in the body in conjunction with other drugs that proved lethal. Overall in Florida, cocaine-related deaths (including the majority of cases where cocaine wasn’t directly the factor but was present in the body at the time of death), have fallen from a peak of 2,179 in 2007 to 1,462 in 2009. (Again, cocaine was the direct result of death in 529 cases out of those).

Ken Kramer, a researcher with the Citizens Commission on Human Rights of Florida, says the numbers underestimate the extent of the problem, because medical examiners do not track deaths attributed to antipsychotic drugs or to antidepressants, both of which carry black-box or black-label warnings. The warnings on antidepressants, required by the Food and Drug Administration, state that the drugs increase the risk of suicidal thinking and behavior in children, adolescents and young adults up to age 24. (Antidepressants include Paxil, Prozac, Zoloft, Effexor, Lexapro and Celexa.)

Anti-psychotic drugs carry a variety of black label warnings of increased mortality in elderly patients (including a death rate almost twice as high for people taking Risperdal, for example). Those drugs, prescribed and often overprescribed in nursing homes and assisted living facilities, include Abilify, Clozaril, Geodon, Risperdal, Seroquel and Zyprexa.

“Certainly, the actual number of prescription drug deaths is higher than the annual report states,” Kramer said. “It is unknown just how much higher because the Medical Examiners Commission does not track these classes of drugs.”

Two years ago Kramer got his concern heard by the commission following an email exchange with a commissioner in which he argued that antidepressants and anti-psychotic drugs’ contributions to mortality should be part of the annual report. He was rebuffed. One examiner vsaid he had not seen “more than the occasional death caused by these types of drugs,” according to the minutes of the Aug. 13, 2008 meeting of the commission.

Read entire article:  http://flaglerlive.com/7256/florida-prescription-drugs-deaths-oxycontin-oxycodone

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