Posts Tagged ‘ADHD’

Psychiatric disease labeling of children exposed as scam by non-profit group

Tuesday, July 26th, 2011

NaturalNews – July 26, 2011

by Bella Muse

Child drugging has been a huge profitable market for Big Pharma, earning them $4.8 billion dollars a year. They have done everything in their power to convince the press, legislators and especially parents why children need to be put on drugs.

They claim that ADD/ADHD, depression, bipolar disorder, etc., are medical conditions, and consider them on par with cancer, diabetes, and heart disease. But in reality there is no actual evidence that proves that psychiatric disorders are indeed medical conditions. They simply diagnose a child by using a behavioral checklist.

There are 20 million children in the United States who have been diagnosed with some kind of psychiatric disorder and drugged for it. It’s practically an epidemic. Innocent children are being turned into patients for simply acting like kids.

Not to mention that all those who are licensed by the government who can “legally” prescribe drugs are paid huge amounts of money by the pharmaceutical industry to write prescriptions of their drugs. But has anyone considered the side effects that these drugs have on children?

In 2001, Matthew Smith, 14, was skateboarding with his cousins when he collapsed and started turning blue. By the time the paramedics arrived Matthew couldn’t be revived and suffered a heart attack.

According to Dr. Ljubisa Dragovic, the cause was Ritalin. Matthew Smith was only six years old when his parents followed the school social worker’s advice and placed him on Ritalin. She claimed Matthew had “ants in his pants” and wouldn’t sit still. After the autopsy, Matthew’s heart showed the same signs of vessel damage that are caused by amphetamines and cocaine.

Ritalin is a methylphenidate, and classified as a Schedule II drug. The DEA reserves it as one of the most dangerous and addictive drugs allowed to be legally prescribed. Some of the serious known side effects are heart palpitations, heart attacks, and cardiac arrhythmia. Why in the world would they prescribe this to children?

What is being done to these kids is truly child abuse. If children are not running around, being loud and constantly playing, then I’d be concerned. Forcing them to sit still and act like adults is unrealistic and cruel.

There’s so much that we can learn from our children if we stop and observe them. They are always in the moment. All they require is patience, understanding, and love. Not drugs.

Online resources:

The Fraudulent Nature of Psychiatric Labels Exposed by Human Rights Group

www.cchrint.org/2011/04/25/the-frau…

www.feingold.org/Research/ritalin.html

www.myhealthtoday.com

www.ritalindeath.com

www.chaada.com

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America conned: Psycho pharma drug pushing empire under fire

Tuesday, July 26th, 2011

NaturalNews – July 26, 2011

by Monica G. Young

"psychopharma is looking like an idea whose time has passed."

Is America truly stricken with widespread mental illness? Do tens of millions need mind-altering drugs? A recent flurry of media articles lead readers to a realization that Big Pharma and the “mental health” industry have deceived Americans on a grand scale.

The “New York Review of Books” two-part article by Dr. Marcia Angell, Senior Lecturer at Harvard Medical School and former Editor in Chief of The New England Journal of Medicine, summarizes it extremely well. She analyzes three books by authors Irving Kirsch, Robert Whitaker, and Daniel Carlat. Each deconstructs the apparent mental illness epidemic and theory that mental disorders stem from brain chemical  imbalances which can be corrected by drugs.

Dr. Angell’s review has sparked a host of other journalists to applaud her and fuel the fire. An article in Forbes even concludes, “psychopharma is looking like an idea whose time has passed.”

As an overview:

Ten percent of Americans over age six take antidepressants. Antipsychotic drugs, once reserved for schizophrenics, have become the top-selling class of drugs in the US, with over $14 billion in sales in 2009. ADHD, bipolar and autism diagnoses have exploded in the past two decades with at least 5 million US kids now on psychiatric drugs.  Ten percent of boys take drugs for ADHD. Half a million kids take antipsychotics, including preschoolers.

The chemical imbalance theory rose to fame when Prozac hit the market in 1987, accompanied by massive hype that it corrected a chemical deficiency in the brain. In the years that followed, the number of people prescribed drugs for mental illness skyrocketed. Today, “treatment” for mental disorders is synonymous with psychoactive (mind-altering) drugs.

Tracing the origin of this theory shows it wasn’t that chemical imbalances were discovered in the mentally ill and then drugs were devised to correct the imbalance. Instead, drugs created for other purposes were incidentally found to also affect brain chemicals and blunt mental symptoms. Drug companies, hungry for new markets, and   psychiatry, eager to build stature in the medical arena, leapt on this. They conducted a vast campaign to popularize chemical imbalances as the cause of mental disturbance and push drugs as the answer.

As Dr. Angell writes, “instead of developing a drug to treat an abnormality, an abnormality was postulated to fit a drug.” “Or similarly,” she says, “one could argue that fevers are caused by too little aspirin.”

Many scientific studies disprove the chemical imbalance theory. After fifteen years of research, Irving Kirsch – psychologist and author of “The Emperor’s New Drugs” – concludes, “It now seems beyond question that the traditional account of depression as a chemical imbalance in the brain is simply wrong.” Research studies show psychoactive medications actually disrupt brain chemistry and causes the brain to function abnormally. This year prominent neuroscientist, Dr. Nancy Andreason, announced proof that antipsychotics shrink the brain.

Studies also demonstrate that long-term recovery rates are higher for nonmedicated patients. For instance, the World Health Organization conducted an investigation in fifteen cities around the world and out of 740 depressed individuals studied, those that weren’t on psychiatric drugs had the best long term outcomes.

In the pre-medication era, it was known that with time, people usually recovered from depression. If kids had tantrums, were unruly or shy, they were apt to outgrow it. Today, individuals branded with disorders are likely to receive long-lasting diagnoses, endless prescriptions and the poorer ones tend to remain on disability for life.

Big Pharma manipulation

Dr. Marcia Angell says the author of each of the three books agrees on “the disturbing extent to which the companies that sell psychoactive drugs – through various forms of marketing, both legal and illegal, and what many people would describe as bribery – have come to determine what constitutes a mental illness and how the disorders should be diagnosed and treated.”

According to IMS Health, an information and consulting company, pharmaceutical companies spent $6.1 billion in 2010 in marketing to US doctors. Another $4 billion was spent on direct-to-patient advertising.

Drug trials, used to bring a drug to market, are funded by drug companies, heavily biased and misleading. Companies may sponsor as many trials as they like until they have just two positive ones to submit to the FDA. Great care is taken to hide negative trials. The highly positive results of placebo trials are downplayed: a high percentage of patients recover on a fake drug (like a sugar pill) – proving that the more a person believes he will benefit from a treatment, the more likely he will experience a benefit.

In regards the Diagnostic and Statistical Manual – the psychiatric bible of mental disorders, used in prescribing drugs – Dr. Angell points out “in all of its editions, it has simply reflected the opinions of its writers.” The majority of the psychiatrists involved in creating the current edition had financial ties to drug companies.

Author Daniel Carlat points out that “psychiatrists consistently lead the pack of specialties when it comes to taking money from drug companies.”

Crime against humanity

And where has the “mental health” industry and “drug therapy” brought our nation?

As Americans line up at their local pharmacy, documented side effects are legion: weight gain, deadened emotions, diabetes, heart problems, liver damage, stunted growth in kids, shortened life spans and on and on. Those prescribed one psychoactive drug are commonly prescribed another to address side-effects, with many on daily cocktails of meds.

An estimated 2.2 million Americans are hospitalized each year for adverse drug reactions. Over 100,000 die from them.

Instead of decreasing, the number of adults on disability pay for mental illness has soared 250% since 1987 and for kids it’s a 35X increase.

The greatest  crime to humanity is the mass drugging of children. Yet it’s perpetrated within schools, doctors offices, foster homes and juvenile facilities daily.

There is good news. In the past few years, drug companies have faced a rise of multi-billion dollar class action suits. The key popularizer of childhood bipolar and antipsychotics for kids, Dr. Joseph Biederman, was publicly sanctioned by Harvard Medical School for failing to report $1.6 million he pocketed from drug companies. Some drugmakers are steering away from pursuing new psychoactive drugs.

Nazi chief propagandist Joseph Goebbels once said, “If you tell a lie big enough and keep repeating it, people will eventually come to believe it.”

This chemical-imbalance/drug therapy lie has been told big enough and repeated enough, that much of America believes it. Isn’t it time we all put a stop to it?

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Attention deficit disorder gurus in conflict of interest

Friday, July 15th, 2011

The Australian – July 14, 2011

by Sue Dunlevy

TWO of the seven experts advising the government on national guidelines for Attention Deficit Hyperactivity Disorder have links to ADHD drug companies, new conflict-of-interest declarations show.

Westmead adolescent health expert Michael Kohn, who has been appointed to the National Health and Medical Research Council working group, was paid by Eli Lilly, the maker of the ADHD drug Strattera, to develop educational material.

And Janssen-Cilag, which makes the ADHD drug Concerta, gave funds for Professor Kohn to go to a Beijing conference on mental health and to produce teaching material.

Claims have been made that some experts advising the government on ADHD have links to drug companies. Source: The Daily Telegraph

The consumer representative on the committee, Margaret Vikingur, the president of Learning and Attentional Disorders, says her organisation received $5000 from three drug companies to develop educational materials.

More than 400,000 ADHD prescriptions a year are written, and their use has soared by 300 per cent over the past seven years, sparking debate about use and conflicts of interest.

Drug firms told Medicines Australia they spent more than $40 million wining and dining and “educating” doctors in the six months to March last year.

The conflict-of-interest declarations will be made public today by Mental Health and Ageing Minister Mark Butler, and follow the controversy over the 2009 draft ADHD guidelines, which were never adopted by the NHMRC because of concerns US research heavily cited in them was compromised by drug firm funding.

US psychiatrist Joseph Biederman, whose work is cited over 80 times in the draft guidelines, and two colleagues were sanctioned by Harvard University after allegedly failing to report more than $1.6m they received from drug firms.

The 2009 ADHD guidelines will be redeveloped.

“I am committed to ensuring the clinical practice points developed by this group will not be influenced by undeclared or inappropriate conflicts of interest,” Mr Butler said yesterday.

West Australian Labor MP Martin Whitely said the conflicts of interests declared by Professor Kohn and Ms Vikingur should have had them excluded from the panel.

http://www.theaustralian.com.au/national-affairs/health/attention-deficit-disorder-gurus-in-conflict-of-interest/story-fn59nokw-1226093390142

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ADHD review as US expert faces inquiry

Tuesday, July 5th, 2011

The Australian – July 5, 2011

AUSTRALIA’S ADHD guidelines are being redeveloped as a US psychiatrist whose work is heavily cited in existing draft guidelines has been sanctioned by Harvard University for violating conflict-of-interest rules.

Professor Joseph Biederman and two colleagues, Thomas Spencer and Timothy Wilens, were investigated by Harvard after allegedly failing to report to the university millions of dollars they received from drug firms.

Australia’s National Health and Medical Council held off approving the draft guidelines for Attention Deficit Hyperactivity Disorder issued in 2009 as it awaited the outcome of the US conflict-of-interest investigation.

The Boston Globe reported that, in a letter to their colleagues, Professor Biederman, Dr Spencer and Dr Wilens apologised for their “honest” mistakes and said they had been sanctioned.

The National Health and Medical Research Council said yesterday it could not yet assess the impact of the outcome of the Harvard investigation on the scientific literature and said the draft guidelines citing Professor Biederman would remain on its website.

Independently of the Harvard review, the council had appointed a multi-disciplinary panel to develop new clinical practice points to provide clear advice to clinicians and health professionals for the diagnosis and treatment of ADHD, the council said.

The review will be completed in September, but the council was last night unable to provide The Australian with names of the experts involved.

In 2007, Daryl Effron, who chaired the committee that drew up Australia’s draft ADHD guidelines, resigned as chairperson after his ties with pharmaceutical companies that produce ADHD drugs were exposed. He remains on the committee.

About 350,000 Australian children and adolescents are estimated to have ADHD and controversy has been raging about the use of medications such as Ritalin.

Child psychiatrist Professor Jon Jureidini, who argues against the long-term use of stimulant drugs in treating behavioural problems tagged as ADHD, says that the current guidelines rely heavily on Professor Biederman’s work.

http://www.theaustralian.com.au/news/nation/adhd-review-as-us-expert-faces-inquiry/story-e6frg6nf-1226087514583

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Bad Side-Effects Ahead For Pharma?

Thursday, June 30th, 2011

Forbes – June 30, 2011

by Martin Fridson

In 2006, The New York Review of Books reported that four-year-old Rebecca Riley died of the effects of two prescription drugs—Clonidine and Depakote.

These medications, along with Seroquel, were prescribed for Rebecca after she was diagnosed, at the age of two, with attention deficit hyperactivity disorder (ADHD) and bipolar disorder.  The three drugs are not approved by the Food and Drug Administration (FDA) for treatment of ADHD or long-term treatment of bipolar disorder, nor are they approved for children as young as Rebecca.

The New York Review of Books‘ recent two-part article (1)  by Marcia Angell on the treatment of mental illness with psychoactive drugs (those that affect the mental state) addresses an issue that may one day prove very important to investors in pharmaceutical stocks.  (All statistics and quotations herein are drawn from Dr. Angell’s article.)

It is not illegal for a doctor to prescribe a drug off-label, that is, for a non-FDA-approved use, but a drug marketer cannot lawfully encourage a doctor to do so.  The profits in psychoactive drugs, however, make it tempting to flout the law.  In the past four years, AstraZeneca (AZN), Pfizer (PFE), Eli Lilly (LLY), Bristol-Myers Squibb (BMY) and Forest Labs (FRX) have all settled federal charges of marketing psychoactive drugs off-label, at a cost running into hundreds of millions.

Seeing that pharmaceutical marketing executives are evidently undeterred by the law, Dr. Angell, a senior lecturer in social medicine at Harvard Medical School and former editor in chief of The New England Journal of Medicine, advocates a prohibition on prescribing psychoactive drugs off-label.

A ban would cut into a major growth area for pharmaceutical companies.

This growth is not a function of a few blockbuster drug discoveries. It parallels an extraordinary rise in the portion of the population, particularly children, diagnosed with mental illness.  For example, if diagnoses mirror the actual incidence of juvenile polar disorder, that affliction grew forty-fold between 1993 and 2004.

Have mental disorders genuinely proliferated that dramatically?  Dr. Angell suggests instead that the surge in certain diagnoses reflects a long-run shift in emphasis from “talk therapy” to medication.  This change just so happens to enable psychiatrists to see more patients and earn higher fees.  Not incidentally, with drugs now regarded as the preferred mode of treatment, the increase in diagnoses is a boon to pharmaceutical manufacturers.  The new generation of psychoactives has displaced cholesterol-reducing medications as the biggest-selling class of drugs in the U.S.

Also benefiting from the present arrangement are low-income families that receive Supplemental Security Income (SSI) payments on the basis of mental disabilities.  To qualify, applicants (children included) generally must be taking psychoactive drugs.  Getting into the program usually also ensures that the family will qualify for Medicaid.  The disbursements can be so substantial that MIT economics professor David Autor describes SSI as “the new welfare.”

The parents and two siblings of Rebecca Riley, the four-year-old who died from the effects of off-label drugs, were all on psychoactive drugs and were receiving about $30,000 a year from SSI.  Dr. Angell links the astonishing rise in diagnoses of certain mental disorders to the huge financial stakes of physicians, pharmaceutical companies and SSI recipients.

I do not want to portray this issue as an imminent or mortal threat to pharmaceutical stocks. If a ban on off-label prescription of psychoactive drugs were proposed in Congress, the companies’ lobbyists probably could stave it off for a long time.  Furthermore, the major pharmaceutical companies have widely diversified product lines, so a setback in the psychoactive category, even though it is a major growth area, would not be a body blow.

Still, this topic is one to keep an eye on for investors who hope to gain an edge by seeing beyond the quarterly EPS data.  Psychoactive drugs have been around since the 1950s, but parents can readily observe that their use with children is far more widespread than it was a generation ago.  If advocates such as Marcia Angell can make a persuasive case that the change is not fully justified on medical grounds, yet poses significant health hazards, is it unrealistic to expect a public opinion backlash some day?

[1] Marcia Angell, “The Epidemic of Mental Illness: Why?” The New York Review of Books (June 23, 2011), pp. 20-22 and “The Illusions of Psychiatry” (July 14, 2011), pp. 20-22.  The article is a review of three books on the contemporary practice of psychiatry by Irving Kirsch, Robert Whitaker, and Daniel Carlat.

http://blogs.forbes.com/investor/2011/06/30/bad-side-effects-ahead-for-pharma/

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Ritalin for children is “quick fix” and should be reviewed, demand educational psychologists

Wednesday, June 15th, 2011

Psychminded.co.uk
By Angela Hussain
June 15, 2011

Ritalin and other psychotropic medication for children are a “quick fix” and the government should urgently review their use, psychologists have urged.

The Association of Educational Psychologists (AEP) fears there is insufficient data on the effects such drugs have on child development. Further research is urgently needed, it says.

The AEP’s demand is despite the fact that a European Medicines Agency (EMA) investigation into methylphenidate drugs, which include psychotropics Ritalin, Concerta, Equasym, Medikinet and Rubifen – had previously stated that the benefits of such drugs outweigh any negative effects for children diagnosed with ADHD and other conduct disorders..

Plus, UK doctors have been advised by the National Institute for Health and Clinical Excellence not to prescribe methylphenidate as a first-line treatment for children diagnosed with ADHD.

But the AEP – which represents UK educational psychologists – fears there will be an increase of methylphenidate prescribing because the number of official psychological disorders for children is set to increase.

The American Psychiatric Association is working on its 2013 Diagnostic and Statistical Manual of Mental Disorders (the DSMV) in which additional psychological disorders for children are due to be added. These include Posttraumatic Stress Disorder in Preschool Children, Temper Dysregulation Disorder with Dysphoria, Callous and Unemotional Specifier for Conduct Disorder, Non-Suicidal Self Injury, and Non-Suicidal Self Injury Not Otherwise Specified.

“These could lead to more young people being referred for treatment with these [psychotropic] medications,” said Kate Fallon, AEP’s general secretary.

She said: “There is a danger that we rely on the ‘quick fix’ for children with conditions such as ADHD, which frequently means the prescription of medication such as Ritalin instead of a number of other possible interventions.”

Medicine regulators in European member states had in 2007 requested EMA’s mediation because of concerns over cardiovascular and cerebrovascular effects of methylphenidate – such as heart rate and blood pressure increases and heart attack.

A review was carried out by the EMA’s committee for medicinal products for human use. It was based on reported side effects and all studies on methylphenidate since the fifties.

The committee also investigated any link between methylphenidate and psychiatric problems, reduced growth and sexual maturation.

An urgent restriction to methylphenidate prescribing was not needed, the committee concluded.

http://psychminded.co.uk/news/news2011/june11/Ritalin-for-children-is-quick-fix-and-should-be-reviewed-demand-educational-psychologists001.html

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Child victims of the chemical cosh: Boy who killed himself after taking Ritalin

Monday, June 13th, 2011

The Daily Mail – June 13, 2011

by Sue Reid

“This doctor said at the inquest my son had a chemical imbalance in his brain. I asked him: “How do you know? Did you take chemicals from his brain? ‘He told me it was a theory. So based on a theory — and seeing my son five times at the most — he decided to put him on this drug, Ritalin, which is as powerful as cocaine.”       – Darren Hucknall

Boisterous: Harry Hucknall was, says his father, a 'normal kid' whose problems were overstated

Captured in a family video, Harry Hucknall gives a cheeky grin before whizzing off down the street on his new bike. His father, Darren, will never forget the moment — when Harry was seven — and often watches the scene again and again.

It is a precious memory of Harry who, one Sunday evening in September last year, kissed his mother Jane and older brother, David, goodnight before going upstairs to his bedroom and locking the door. He then hanged himself with a belt from his bunk bed.

He was ten years old.

His father blames Harry’s death on two ‘mind-altering’ drugs that his son had been prescribed by a psychiatrist to cure his boisterous behaviour and low spirits.

An inquest was told in April that the boy had more drugs in his body than the normal level for adults suffering from the same problems.

Now, a distraught Mr Hucknall is to make a formal complaint to the NHS for prescribing his son Ritalin, a cocaine-like stimulant which, paradoxically, is said to calm down a child, and Prozac, a powerful antidepressant.

‘When I was growing up there were lots of kids like Harry — a bit over-active, a bit naughty, who didn’t always do as they were told. Now they are branded with a complaint called attention deficit hyperactivity disorder,’ says the computer engineer at his semi-detached house on the outskirts of Barrow-in-Furness, Cumbria.

‘What is it? What has changed? Is there some weird disease in the air? Harry was just a normal little boy. But because we live in 2011 he, and many other kids, are on tablets.

‘It seems nearly every child has suddenly developed this ADHD. What a load of nonsense. It’s an easy get-out for parents and schools who can’t control children.’

Mr Hucknall is obviously grieving for Harry, and his words are spoken with anger. But they are close to the truth. Earlier this year, this paper revealed that 661,000 prescriptions are dished out annually in Britain to treat childhood ADHD — double the figure of five years ago.

Coroner: An inquest was told in April that the boy had more drugs in his body than the normal level for adults suffering from the same problems

These medicines are being given to very young children — one aged just 15 months, according to our investigations — despite official guidelines from the manufacturer and the fact that the UK’s National Institute for Health and Clinical Excellence (NICE) prohibits their use for those under six.

Last week, educational psychologist David Traxson told me he suspects that in the West Midlands at least 100 three, four and five-year-olds are on Ritalin or similar drugs. If this is replicated around the country — as is likely — the number will run into thousands.

‘These young children are taking powerful, potentially addictive drugs and no one knows what will happen to their brains in the future,’ he warned.

The Association of Educational Psychologists last week demanded a national review into the use of Ritalin and similar drugs on children.

General Secretary Kate Fallon said: ‘The danger is that we rely on this “quick fix” for children with conditions such as ADHD, which frequently means a prescription for Ritalin.

‘No one’s certain what it will do to children’s brains’

‘We have significant concerns that the neurological impact of these drugs on the developing brains of children has not been fully researched. The potential damage they could cause needs further investigation.’

In America (where the term ADHD was first created 50 years ago), one in five children is diagnosed as having a hyperactivity disorder and is on Ritalin or a similar drug

The psychologists’ call was backed by the National Union of Teachers, whose members have to cope with the huge rise in pupils being dosed with ADHD drugs — which act on the central nervous system to change a child’s behaviour.

In some state primary classrooms, one in ten pupils is on Ritalin pills, which have to be handed out by teachers at lunch or break times. In one junior school of 389 children in the South-East, no fewer than 80 pupils — more than 20 per cent — are on the medication.

It is a phenomenon across Britain, affecting families in every income bracket. The area with the highest proportion of children receiving the drug is the Wirral, a wealthy part of Cheshire which is home to millionaire footballers and business executives.

Meanwhile, sceptics question the very existence of ADHD as an illness. There is no recognised test for it. A diagnosis is made by a psychiatrist or paediatrician merely by watching a child’s behaviour.

Some of the doubters argue the condition is really a politically correct creation, conjured up by the medical world for a child who finds it difficult to sit still or concentrate thanks to a combination of a fast-food diet, late nights and lack of exercise.

It’s easier for the medical world and its political masters, of course, to diagnose a syndrome rather than deal with the real causes.

Another worrying factor is that the parents of children receiving drugs for ADHD immediately become eligible for an array of generous state benefits, including a carer’s allowance and child-disability allowance, which can total thousands a year.

For instance, one family in the West Midlands has two children receiving medication for ADHD. They get £600 a month in disability allowances for each of the two children who have been diagnosed with the ailment.

A third child is being examined by psychologists to see if he is also a sufferer. If he is diagnosed, the family’s annual haul from the state will be £21,600 tax free.

No wonder thousands of families happily agree with child psychiatrists when they are told their son or daughter needs medicine to ‘cure’ their hyperactive behaviour.

Gwynedd Lloyd, an education researcher at Edinburgh University, has explained her doubts. ‘You can’t do a blood test to see if a child has ADHD. It is diagnosed by ticking a behaviour checklist — getting out of your seat and running about is an example. Half the kids in a school would qualify under these sorts of criteria.’

And, it appears, a lot of them do. In the four years to 2010, there was a  65 per cent increase in NHS spending on drugs to treat childhood ADHD, with a cost to the taxpayer of £31million annually. This does not take into account thousands of prescriptions paid for by parents who take their children to private doctors.

In America (where the term ADHD was first created 50 years ago), one in five children is diagnosed as having a hyperactivity disorder and is on Ritalin or a similar drug.

It is predicted that unless the craze for drugging children is not stopped in the UK, one in seven pupils will soon be diagnosed with the condition in many parts of the country, as is already the case in places such as the Wirral.

‘Doubters say it’s an illness conjured up by medics’

Meanwhile, the side-effects of the ADHD treatments are legion. Ritalin is a Class B drug, which is banned for recreational use. It was invented in the Fifties in the U.S. to combat the effects of illegal drug overdoses.

Alarmingly, it can stunt growth (doctors are asked to regularly monitor a young patient’s height and weight), while making children prone to heart problems, depression and insomnia.

At least 11 deaths of children while taking Ritalin have been reported to the UK’s Medicines and Healthcare Products’ Regulatory Agency since the drug became available 20 years ago. The official causes of nine of the deaths included heart conditions, respiratory problems and brain diseases. Significantly, two of the children ended their own lives just like Harry Hucknall.

'Enough is enough': Home Secretary Theresa May has warned of the dangers of the ADHD drugs

Home Secretary Theresa May has said that enough is enough. As the Shadow Leader of the House of  Commons before the last election, she warned of the dangers of the ADHD drugs. ‘They are powerful prescription drugs and we don’t know what their long-term effects on a child will be.’

She related to Parliament the story of a six-year-old on Ritalin. ‘He experienced low moods and marked depression and tried to throw himself out of a window within two months of starting treatment. He only recovered once the drug had been withdrawn.’

Sadly, Harry Hucknall never had the chance to stop taking Ritalin, or the antidepressant Prozac. Now his father is asking difficult questions about why his son died. On the fateful weekend last September, Harry was staying at the home in Dalton-in-Furness of his mother, Jane White, 33, his brother David, and his two step-siblings.

In America (where the term ADHD was first created 50 years ago), one in five children is diagnosed as having a hyperactivity disorder and is on Ritalin or a similar drug

He would spend every other weekend and one day during the week with his father, who parted amicably from Jane when Harry was three.

Early last year, child psychiatrist Mr Sumitra Srivastava had prescribed Harry with Prozac for depression, and Ritalin for hyperactivity. He was having difficulty concentrating at school, was being bullied by classmates, and had told his parents he was feeling unhappy.

At an inquest in April, the coroner Ian Smith declared that Mr Srivastava had acted appropriately, but warned that doctors should be extremely careful what they prescribed to ten-year-old boys.

The coroner ruled out a deliberate suicide, but said that the influence of Ritalin and Prozac could not be excluded as a factor in Harry’s death. ‘What a child with ADHD is prescribed by his doctor is mind-altering drugs of a powerful nature,’ he added.

But Harry’s father believes drugs had a huge part to play in the tragedy. ‘Harry was put on Prozac first, and without my knowledge,’ he told me. ‘I only found out about it when he came to stay for the weekend and his mother told me what dose to give him: one in the morning and one at night. “Are you crazy?” I asked her. “That’s an antidepressant.”

‘I can go to work every day and pay for my child’s keep, but it seems I have little say when it comes to things like the authorities deciding to give my son drugs.’ At first, Mr Hucknall refused to give Harry the pills. But Harry’s mother said that if he didn’t dose his son, the child would not be allowed to visit him. She said the doctors had told her Prozac would stop Harry being depressed.

‘I reluctantly agreed. I wanted to see Harry,’ remembers 37-year-old Mr Hucknall. ‘Later, I went with Harry’s mother to see the psychiatrist. I insisted on going along to tell him that I did not want Harry on any drugs whatsoever.

‘While I was there, he said Harry was going to be put on Ritalin as well. I said I did not want him on more drugs. I didn’t want him  on any at all.

‘I had never heard of Ritalin. I was told it was to help his concentration. I was never told a side-effect of Ritalin is depression. But the doctor said that if Harry took the Ritalin he would be off everything and drug free within a month.’

Mr Hucknall believed him, although this scenario was very unlikely. Most children remain on ADHD drugs for years. ‘In the end I agreed, because I thought I was doing the right thing. The next thing I know, a month or two later, there was a knock on my door and two police officers were telling me my son had  hanged himself,’ he says.

‘He was just a kid. There was nothing wrong with him. He may have had some problems, but they were overstated.

‘A lot of things that Harry’s mum complained about in terms of his behaviour, he did not do here. How can you have ADHD in one place and not in another?

‘I think Harry might have been playing up a bit by attention- seeking because there were three other children in the family.

‘I admit there were a couple of times I forgot to give him his  tablets. To me, he seemed quiet and subdued when he was on them.

‘I would have happily thrown them in the bin. Harry just took them, of course. He was a kid and he did as he was told.’

An emotional Mr Hucknall continues: ‘I think ADHD is a disease invented by drug companies. Nobody ever died of ADHD and it didn’t existed once upon a time. It’s too easy to hand out tablets. They are being over-prescribed to children.

‘A perfectly normal kid isn’t allowed to grow up without interference these days. I’m angry about what has happened because I have lost my son.

‘At the school meetings about Harry, his teachers said he was quiet. My son had just recently moved house and been put into a new school, where he didn’t know anybody. What did they expect?

‘Another teacher said Harry didn’t laugh at his jokes. I asked Harry about that. He told me they weren’t very funny.’

Mr Hucknall believes his son was ‘inappropriately medicated’ and has asked Independent Complaints’ Advocacy Service (ICAS) — which supports those wishing to complain about the NHS — to take on the case.

At the inquest, Mr Hucknall also took the chance to challenge Mr Srivastava again about why he had put Harry on drugs. ‘This doctor said at the inquest my son had a chemical inbalance in his brain. I asked him: “How do you know? Did you take chemicals from his brain?”

‘He told me it was a theory. So based on a theory — and seeing my son five times at the most — he decided to put him on this drug, Ritalin, which is as powerful as cocaine.

‘Harry ended up taking two drugs that work against each other — the Prozac that fights depression and the Ritalin that can cause it. How can that be right?’


Note from CCHR:  If you want to  help inform parents of the actual documented dangers of psychiatric drugs from international drug regulatory agencies — help distribute this video, which links to our psychiatric drug side effects database:

Drugging Kids - Side Effects

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At annual convention, psychiatrists collaborate on mental disease mongering to boost profits

Wednesday, June 8th, 2011

Natural News – June 8, 2011

by Monica G. Young

While sipping drinks from coconut shells, psychiatrists from around the world recently met in Honolulu to discuss more ways to capitalize on human behavior and promote drug dependency. The occasion was the annual meeting of the American Psychiatric Association (APA), held in a Hawaiian convention center lined with mental disorder displays and pharmaceutical booths.

“Hot” topics (potential markets for social control and drug pushing) included:

1) Mental health issues during a woman’s reproductive cycle, such as “treating” pregnant women for bipolar – a disorder said to cause unusual shifts in mood and energy levels. In speaking to Medscape News, an APA committee co-chair, Dr. Don Hilty, called this “a really nice-growing area.”

Yet most every woman experiences mood and energy shifts during pregnancy. Despite this, it is not uncommon for pregnant women to be diagnosed as bipolar and prescribed antipsychotics, some of the most powerful drugs on the market. Even the FDA website alerts doctors to “be aware of the effects of antipsychotic medications on newborns when the medications are used during pregnancy.” The site warns of abnormal muscle movements and withdrawal symptoms, and the FDA’s adverse effects reporting program (Medwatch) includes cerebral hemorrhage, heart malformations and death as documented reactions in newborns. Similarly, studies show birth defects and other serious risks for infants whose mothers took antidepressants while pregnant.

2) Childhood disorders were a particularly popular issue at the convention. But they didn’t stop there – prenatal and newborn genetic screening for mental illness has taken on new emphasis in the psychiatric world. “It’s also trying to understand how genetics predict what medications can be used,” stated APA’s Dr. Hilty.

Having already labeled millions of kids “abnormal” and drenched their brains in toxic substances – a multi-billion dollar business – apparently they aren’t satisfied. They aim to brand children as mental patients and destine them for drug-dependency before they’re even born.

The conference even touched upon electroconvulsive shock therapy (ECT) for children – sending electric volts through their heads. That will teach ‘em to shut up and sit still! It will also cause permanent brain damage.

3) ADHD is usually promoted as a childhood disorder but a team of psychiatrists proposed a new definition to make it easier to diagnose (and drug) older teens and adults. They claim people who tend to miss work deadlines and interrupt others deserve this label.

This would surely lead to millions more on daily meds. Who doesn’t know co-workers who miss deadlines or even friends who interrupt you? Not emphasized however is that, per a study published in The Clinical Neuropsychologist, one in four adults seeking an ADHD diagnosis fake it to obtain stimulant drugs.

4) Capitalizing on America’s service men and women was another hot one: diagnosing and drugging the military for post-traumatic distress disorder, depression and anxiety.

Did they mention that 18 U.S. veterans commit suicide daily, largely due to psychiatric drugs? Not likely. As reported by Neev M. Arnell in NaturalNews, “the increasingly high number of deaths among both veterans and active duty soldiers-including suicides, accidental overdose, and lethal drug interactions-have now been linked to the exponential increase in the prescribing of drugs for post traumatic stress disorder, depression and other psychological illnesses.” (http://www.naturalnews.com/032598_v…)

5) Anticipating the “silver tsunami” as the Baby Boomer generation moves into the over-65 bracket, psychiatrists stressed the need for more psychiatric services for the elderly.

Not stressed, if mentioned at all, is the rampant over-use of psychiatric drugs in nursing homes. Elderly patients’ reactions to physical ailments are often squelched with mind-altering drugs. And a recently released government audit shows nearly one in seven elderly nursing home residents are given antipsychotics – nearly all of them dementia patients for whom the drugs can be lethal. Many lawsuits and settlements have revealed that drug companies have falsely promoted these drugs to doctors and nursing homes for years.

6) While not on the “hot” list, another issue that bit was bedbugs. A New York psychiatrist and his colleagues presented a detailed study showing bedbugs can trigger anxiety.

What a remarkable – and potentially profitable – discovery! Gee, with the rise in bedbug infestation in New York City, maybe Bedbug Anxiety should be included in the next edition of the DSM (psychiatry’s diagnostic and billing bible).

Father of psychiatry – the bloodletter

The American Psychiatric Association calls itself “the voice and conscience of modern psychiatry.”

Adorning the convention hall was the APA logo which enshrines Dr. Benjamin Rush (1746-1813) as the father of psychiatry. A very influential doctor, teacher and statesman of his time, Rush propagated his theory that Blacks suffered from an inherited disease called “Negritude.” The only evidence of a cure, he said, was the skin turning white. He warned, “whites should not intermarry with them, for this would tend to infect posterity with the ‘disorder.’” Whites, seeking not to be “infected,” used this fabled disease to justify segregation.

Rush was also a chief proponent of bloodletting as a cure-all for mental and physical illnesses. Widespread in America in those days, he made lots of money at it. One of Rush’s students applied his teachings to a patient who complained of a sore throat: nine pints of blood were removed from the man’s body in twenty-four hours and he died. That patient was George Washington, the first President of the United States.

Sources for this article include:
http://www.medscape.com/viewarticle…

http://www.medscape.com/viewarticle…

http://healthland.time.com/2011/05/…

http://healthland.time.com/2011/04/…

http://www.nytimes.com/2011/05/10/h…

http://www.jstor.org/pss/985399

http://www.websters-online-dictiona…

http://www.cchr.org/cchr-reports/cr…

About the author:
Monica G. Young is a human rights investigator and educational writer with a purpose to expose the truth about the pharmaceutical and psychiatric industries and safeguard human liberty. She encourages non-drug alternative approaches based on healthy lifestyles and human decency. She supports the Citizens Commission on Human Rights and like-minded groups.

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The business of ADHD

Wednesday, May 25th, 2011

SFGate.com City Brights Blog
By Winston Chung, Child Psychiatrist
May 24, 2011

Psychiatrists convened in sunny Honolulu for the 164th Annual Meeting of the American Psychiatric Association (APA) last week, discussing, among other things, moving forward with plans to make the diagnostic criteria for ADHD less stringent: proposed changes include reducing the number of required symptoms from 6 to 4, for adults and teens, and increasing the age-of-onset criteria from 7 to 12.

Russell Barkley, Ph.D., and Joseph Biederman, M.D., have written about abandoning or generously broadening age-of-onset criteria, arguing that the current, precise age-of-onset criteria poses “unwarranted practical problems for the study of older adolescents and adults.” These two men are considered ADHD experts and contributed to the American Academy of Child and Adolescent Psychiatry (AACAP) Practice Parameters for ADHD, which serve as guidelines by which most child psychiatrists practice.

According to a story from the New York Times, Joseph Biederman did not tell university officials about more than a million dollars received from drugmakers from 2000 to 2007, and he promised Johnson & Johnson research results that would benefit the drug company. On the list of AACAP Conflicts of Interests for Practice Parameters not listed in the Practice Parameters, Russell Barkley receives or has received research support, acted as a consultant and/or served on a speaker’s bureau for Eli Lilly and Company and Shire Pharmaceuticals Group.

Shire Pharmaceuticals Group has a substantial focus on ADHD meds, and they have been pulling out all the stops to try and turn a profit in the face of competition from generic drugs.

Earlier this month, Reuter’s Health described how drugmakers, including Shire, have raised prices to make up for lack of new products and loss of patent protection.

“Prices were just shoved up every year to make more money and meet earnings, to be blunt,” Shire (SHP.L) Chief Executive Angus Russell said.

Shire’s CEO also indicated that the FDA is supporting their plan to study the use of their ADHD drug, Vyvanse, for use in depression and schizophrenia, hoping for billions of dollars in extra sales through expansion of potential indications. Amphetamines for schizophrenia? Hmmmm…..

Jim Edwards of BNET wrote about Shire increasing the price of one of their own ADHD drugs, Adderall XR, to encourage users to switch to their branded, cheaper and newer ADHD drug, Vyvanse, leading to increased sales.

Shire somehow sold more ADHD drugs during a recent, national shortage of ADHD medications – their sales of Adderall XR increased 21 percent in the first quarter of 2011 – a time when many of the patients in San Francisco’s public mental health system were unable to receive their regular ADHD medications.

BNET posted excerpts of separate lawsuits filed by Impax and Teva, manufacturers of generic forms of Adderall XR. They claim that Shire did not honor their contracts and hoarded product for themselves during this recent shortage. In the Wall Street Journal, the associate director of FDA’s drug shortages program reported that this national ADHD drug shortage mostly affected generic forms of ADHD meds. Coincidence?

Other ways of getting around stagnant drug development and generic competition include taking an old drug or active ingredient, and changing the delivery system or duration of action and presenting it as a new, patent-protected product. Here are a few examples that have been associated with Shire:

- Vyvanse: Also known as lisdexamfetamine, Vyvanse is a prodrug of dextroamphetamine. Dextroamphetamine has been used since 1937 to treat hyperactivity in children, so it is hardly new. Vyvanse was marketed as having lower abuse potential – specifically, preventing abuse from snorting, since the prodrug requires digestion to release the active form. In my clinical experience, most abuse of stimulants is due to people taking it without a prescription or shaping their symptoms to get a prescription, and a prodrug likely does little to curb college students from seeking stimulants to study for exams.

- Daytrana: The transdermal methylphenidate (methylphenidate is the active ingredient in Ritalin) patch is worn on the skin and was developed as a way of bypassing the digestive tract, and my experience prescribing this drug was met with equivocal reports from patients and families. I guess there is a reason I can’t remember anyone saying it worked – Shire gave up on the ADHD patch after 9 product recalls and a federal probe.

- Intuniv: An extended release form of guanfacine, Intuniv is touted as a new, non-stimulant treatment for ADHD. But child psychiatrists have been using guanfacine in ADHD for years, and this ‘extended-release’ form has a half-life of about 18 hours, while generic guanfacine has a half-life of about 17 hours – not a robust difference, in my opinion.

I liken these approaches to gimmicks utilized in the mass-produced, beer market: color changing labels to let you know if your beer is cold, wide-mouth beer cans, or vortex bottles. Do any of these ‘innovations’ really change the fact that you’re drinking cheap beer?

As the DSM-V looms closer to becoming a reality, I can’t help but think of words from the man who chaired the committee for the DSM-IV. Allen Frances, M.D., wrote in the in the LA Times:

As chairman of the task force that created the current Diagnostic and Statistical Manual of Mental Disorders (DSM-IV), which came out in 1994, I learned from painful experience how small changes in the definition of mental disorders can create huge, unintended consequences.

Our panel tried hard to be conservative and careful but inadvertently contributed to three false ‘epidemics’ – attention deficit disorder, autism and childhood bipolar disorder. Clearly, our net was cast too wide and captured many ‘patients’ who might have been far better off never entering the mental health system.

The DSM-IV was and the DSM-V will be published by the APA. The same APA that, in 2010, rejected internal recommendations – led by an APA past-president – to regulate or curtail individual psychiatrists’ relationships with the pharmaceutical industry.

Loosening the diagnostic criteria for ADHD, as proposed, will no doubt lead to more people being diagnosed and, inevitably, taking more ADHD drugs. I like to think that the APA and their doctors pushing for the changes are motivated by helping patients and not drug company profits.

After all, if anyone can identify and address unconscious conflicts or psychologically-defended, aggressive drives, it’s a psychiatrist, right?

Read article here:  http://www.sfgate.com/cgi-bin/blogs/wchung/detail?entry_id=89494

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Is ADHD a Fictional Disease?

Saturday, May 21st, 2011

Some psychiatrists argue that ADHD is little more than a marketing gimmick

The Mark
By Fred Baughman
May 18, 2011

Dr. Fred Baughman, Child neurologist; opponent of ADHD diagnosis

Some 5.4 million children in the United States have been diagnosed with attention-deficit hyperactivity disorder, or ADHD, with two-thirds of them taking psychiatric drugs. Sales of ADHD drugs reached $1.2 billion in 2010, a demand level so high that the U.S. is experiencing an ADHD drug shortage. But an increasingly vocal contingent of psychiatric experts is speaking up against diagnosing children with ADHD, arguing it is a non-existent condition drummed up by pharmaceutical companies to increase sales.

What makes you convinced that ADHD is not a real disease?

During my time in practice, I’ve authored papers and discovered real diseases and so on. Psychiatry in 1948 was distinguished from neurology. Neurology is the specialty dealing with physical and organic diseases of the brain and nervous system. Psychiatry is the specialty dealing with emotional and behavioural things which are not actual, physical diseases – things like depression, anxiety, panic, and so on.

Insofar as ADHD is concerned, it seems clear that in the ’50s, as the first psychiatric drugs came to market, that psychiatry – in cahoots with the pharmaceutical industry – came upon the market strategy of, “Well, we’ll call these things ‘diseases.’” And the prototypical invented disease was called ADHD.

It was initially in a 1970 congressional hearing in the U.S. that psychiatrists appeared and testified that, what was then called hyper kinetic disorder or minimal brain dysfunction, was a disease that needed diagnosing by a physician, and as a disease it justified the use of drugs to treat it. So that was the official beginning of ADHD in particular and of psychiatric diagnoses in general as being due to a disease of the brain. In every case, they say there’s a subtle chemical imbalance in the brain, which of course they never have a means of diagnosing in life and have never in scientific literature authored proof that there is in fact a disease. And yet they are allowed by [the U.S.] Food and Drug Administration to say that there is a chemical imbalance and that the drugs balance the imbalance.

So it’s been a market strategy. This lie has been allowed to be published by the drug industry and by psychiatry, by our regulatory agencies, specifically the Food and Drug Administration. So that’s where we are today.

All physicians learn in medical school that a disease is a physical abnormality. When you go to your physician, they may see a rash or they may find something microscopically abnormal, such as cancer cells. Then there are a lot of chemical diseases – diabetes being the best known. There are about a hundred examples of inborn errors of metabolism or body chemistry. These can all be tested for, they’ve all been proven, and they exist in the scientific literature – whereas there is not a single psychiatric diagnosis that exists in scientific literature of the world.

In 2008, I was counselling a young father from Kingston, Ont., who was in a divorce situation, and the mother insisted the children be seen by psychiatrists and the psychiatrist had made a number of diagnoses and had this one boy on large amounts of about five or six different types of medication. I helped the father author a letter to Health Canada asking where – in the case of ADHD or any psychiatric diagnosis – there is proof of a gross or microscopic abnormality.

This gentleman got a letter back from the director-general of Health Canada saying there is no gross, microscopic, or chemical abnormality in any psychiatric diagnosis; there is no objective way of verifying a psychiatric diagnosis as a disease.

That’s why psychiatry’s claims that their diagnoses are chemical imbalances is nothing but a lie and a deception. And yet, because of their financial might on the world scene, no one will challenge them. They have friends bought and paid for in government and in all of the governmental health-care agencies.

Here in the States, as of 2007, the Centers for Disease Control announced that 5.4 million U.S. schoolchildren five to 17 years old had ADHD. And you can be sure that they have all been on ADHD drugs, which are, for the most part, amphetamines, which are known to be addictive, dangerous, deadly.

I’ve heard estimates of 20 per cent of schoolchildren in the U.S. with a psych diagnosis and who were on psych drugs. It’s exploding, it’s increasing all the time.

Is the issue that we’re overmedicating ourselves, or that ADHD is not real?

When it’s a total fraud, you don’t call it overmedicating. There is no such thing as ADHD as a disease, so there is never justification for it. It’s a total fraud.

What is there to gain from diagnosing children with ADHD?

Ritalin has passed $1 billion a year in sales. Ritalin is no longer the top ADHD drug in the U.S. I think Adderall, which is made up of amphetamines, passed Ritalin a few years ago in market share.

It’s a complete fraud, they’ve invented diseases for which their drugs are a cure. The rate of diagnosing ADHD has been going up by a million a year in the U.S. This is a market strategy.

The book Selling Sickness: How the World’s Biggest Pharmaceutical Companies Are Turning Us All Into Patients [by Ray Moynihan and Alan Cassels] talks generally about inventing diseases for which to sell drugs. In the foreword of that book, the authors quote the former president of Merck Pharmaceutical Co., Henry Gadsden, who once said he was anxious to find ways to market his products to normal people, just like the Wrigley chewing gum people did. This was kind of an after-the-fact confession they were trying to market drugs to normal people, and calling all psychological dilemmas diseases for which they needed a pill. This was the strategy.

It’s almost unimaginable, it’s almost unthinkable that this has been going on, but that’s exactly what’s been going on.

How would you diagnose a child that was considered to have ADHD?

Look at the criteria that are used to call a child ADHD. They talk out of turn, they don’t sit still, they wiggle around too much in their seats, they are impulsive, disorderly, and so on. It’s a bunch of behaviours that are seen in just about every child at some stage of their life. This is by design; they have taken kind of irritating, bothersome, disruptive behaviours in children and have kind of cobbled them together and called it a disease.

They get a lot of parents to buy it because a lot of parents are now busy with their job in the workforce and there’s no longer a full-time parent in the home, and so, “Here’s why Johnny or Janey is such an irritant to me, they’ve got ADHD.” It takes the pressure entirely off the parent for not being a presence and for not being there full-time to mould the behaviour of the child, and they’re calling these behaviours a disease and saying we’ve got a pill for it. That’s very seductive. That’s a far more appealing analysis than, “Gee, you’re divorced, there’s no one in the home to discipline the child real time,” and so on.

These are not diseases, they are behaviours. Today, you hang a psychiatric label on a child, you surely stigmatize the child and these drugs are exceedingly dangerous. In 2005, there were several deaths in Canada of young children from Adderall. It was temporarily taken off the market, but then the power of the industry won out and Adderall’s back on the market. Pure amphetamines.

Read article here:  http://www.themarknews.com/articles/5193-is-adhd-a-fictional-disease?page=1

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