Archive for November, 2011

Australia—New Guidelines Threaten Parents Who Refuse to Drug Their Kids

Monday, November 21st, 2011

Note from CCHR: The group that fought for, and won, state legislation in the United States prohibiting schools from being able to force a parent to drug their child as a condition of attending school, was CCHR.     The article does not mention that in the U.S. this bill was also passed on a federal level, the Prohibition on Mandatory Medication Amendment (also due to CCHR’s efforts).   Now it appears Australia is in desperate need of similar legislation.

The Australian – November 21, 2011

EXPERTS have warned that parents who don’t medicate children with ADHD could be referred to child protection authorities under controversial draft guidelines being considered by the National Health and Medical Research Council.

The practice points, to guide doctors who treat the disorder, were drawn up by an NHMRC expert working group to address community concern over the use of stimulant medication to treat attention deficit hyperactivity disorder. They state: “Consideration should be given to the ability of the child/adolescent and their caregivers to implement strategies. As with any medical intervention, the inability of parents to implement strategies may raise child protection concerns.”

West Australian Labor MP, author and anti-ADHD medication campaigner Martin Whitely says “the only possible medical interventions are ADHD drugs and the implied threat that a parent’s refusal to allow their child to be ‘medicated’ with amphetamines may see their child put in care”.

The clinical practice points are open for public comment until the end of the week and he is calling for the statement to be removed because he fears it may lead to a situation similar to that in the US.

Some US states have had to legislate to prevent schools and child protection authorities from telling parents they must put their children on drugs, he said.

However, child psychiatrist and Monash University lecturer George Halasz says the situation should not be seen as unique to ADHD and parents who fail to manage serious conditions such as their child’s asthma or diabetes could also be considered to be failing their duty as a parent.

Dr Halasz said the new guidelines were a step in the right direction because they asked doctors to first try to find other explanations for a child’s behaviour before they diagnosed ADHD.

And he says it will not be humanly possible to diagnose ADHD in a single 50-minute consultation under the new clinical practice points.

“If any child is given medication after one consultation, then that child should be reviewed,” he said.

The practice points state that “a child who meets diagnostic criteria for ADHD may not be best served by making that diagnosis” and says their behaviour may be better understood as a reaction to more specific cognitive difficulties or family/environmental services.

The document says “not all people with ADHD will require, or benefit from, pharmacological management”.

It says children using medication should receive a three- to six-monthly review and that the long-term effects of ADHD drugs are unknown.

However, the document also says “for children and adolescents diagnosed with ADHD, stimulant medications like Ritalin can reduce core ADHD symptoms and improve social skills and peer relations in the short term”.

In the short term, the paper says, “combined behavioural-pharmacological treatment is most effective” in normalising child behaviour.

Controversy has dogged the NHMRC’s ADHD guidelines since Daryl Effron, the original chairman of the committee, resigned because of his association with drug companies that produce ADHD medications.

http://www.theaustralian.com.au/national-affairs/medicate-adhd-kids-or-else-parents-told/story-fn59niix-1226200652633

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Drugs Used for Psychotics Go to Youths in Foster Care

Monday, November 21st, 2011

The New York Times, November 20, 2011

by Benedict Carey

Click image to see video on psychiatric drug warnings for kids

Foster children are being prescribed cocktails of powerful antipsychosis drugs just as frequently as some of the most mentally disabled youngsters on Medicaid, a new study suggests.

The report, published Monday in the journal Pediatrics, is the first to investigate how often youngsters in foster care are given two antipsychotic drugs at once, the authors said. The drugs include Risperdal, Seroquel and Zyprexa — among other so-called major tranquilizers — which were developed for schizophrenia but are now used as all-purpose drugs for almost any psychiatric symptoms.

“The kids in foster care may come from bad homes, but they do not have the sort of complex medical issues that those in the disabled population do,” said Susan dosReis, an associate professor in the University of Maryland School of Pharmacy and the lead author.

The implication, Dr. dosReis and other experts said: Doctors are treating foster children’s behavioral problems with the same powerful drugs given to people with schizophrenia and severe bipolar disorder. “We simply don’t have evidence to support this kind of use, especially in young children,” Dr. dosReis said.

In recent years, doctors and policy makers have grown concerned about high rates of overall psychiatric drug use in the foster care system, the government-financed program that provides temporary living arrangements for 400,000 to 500,000 children and adolescents. Previous studies have found that children in foster care receive psychiatric medications at about twice the rate among children outside the system.

The new study focused on one of the most powerful classes of drugs, antipsychotics. It found that about 2 percent of foster children took at least one such drug, even though schizophrenia and bipolar disorder, for which the drugs are approved, are extremely rare in young children.

“It’s a significant and important finding, and it should prompt states to improve the quality of care in this area,” said Dr. Mark Olfson, a professor of clinical psychiatry at Columbia University who did not contribute to the research.

In the study, mental health researchers analyzed 2003 Medicaid records of 637,924 minors from an unidentified mid-Atlantic state who were either in foster care, getting disability benefits for a diagnosis like severe autism or bipolar disorder, or in a program called Temporary Assistance for Needy Families. All of these programs draw on Medicaid financing. The investigators found that 16,969, or about 3 percent of the total, had received at least one prescription for an antipsychotic drug.

Yet among these, it was the foster children who most often got more than one such prescription at the same time: 9.2 percent, versus 6.8 percent among the children on disability, and just 2.5 percent of those in the needy families program.

Antipsychotic drugs, the authors said, also cause rapid weight gain and increase the risk for metabolic problems in many people, an effect that may be amplified by the use of two at once.

Doctors who treat such children are aware of the trade-offs and often prescribe lower doses of the medications as a result. And when they add a second such drug, it is often to counteract side effects of the first medication.

read the rest of the article here:  http://www.nytimes.com/2011/11/21/health/research/study-finds-foster-children-often-given-antipsychosis-drugs.html?_r=3&adxnnl=1&adxnnlx=1321895404-XjlZbL3lXs10CI4v4o6z6w

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America’s ‘startling’ use of mental-illness drugs: By the Numbers, A Nation of Pill-Poppers

Friday, November 18th, 2011

Note from CCHR: They’re now “trying to figure out” why so many Americans are taking drugs for “mental illness,” but the answer is ridiculously simple: because people are being diagnosed mentally ill for a multitude of behaviors or emotions that have been pathologized into a “disease” by psychiatry & promoted by Big Pharma.  Being sad, anxious, too happy, too sad, in grief,  having to much energy, too little energy, fidgeting, being shy, having too much sex, too little sex, eating too much, eating too little…the list goes on and on.  And that is the reason.  Because there are 374 ways to label you mentally ill… and the number is growing.

THE WEEK – November 18, 2011

A pharmacist counts and divides Prozac prescription pills: 29 percent more women are using antidepressants now than ten years ago. Photo: Paul Skelcher - Rainbow/Science Faction/Corbis

Americans are taking a “startling” amount of mental-health related medications, according to a big new study by Medco Health Solutions. More than 1 in 5 Americans now takes at least one drug to treat a psychological disorder, ranging from antidepressants like Prozac to anti-anxiety drugs like Xanax. Understanding why Americans are taking more pills to treat mental illness “is the next critical goal,” says Dr. Martha Sanjatovic in a statement released by Medco. Here’s a look this growing trend, by the numbers:

2.5 million
The number of Americans surveyed for prescription drug use from 2001 to 2010

1/5
One out of every five U.S. adults takes drugs to treat some type of mental health condition

22
Percent increase in the number of U.S. adults taking mental health drugs in 2010 compared to 2001

29
Percent increase in the number of women using antidepressants in 2010 compared to 2001

1/5
Proportion of women over the age of 20 who are prescribed antidepressants, like Zoloft and Lexapro

11
Percent of middle-aged women using anti-anxiety medications

5.7
Percent of middle-aged men using anti-anxiety medications

3
Number of people ages 20 to 44 using antipsychotic drugs (like Resperadol) and ADHD medications (like Ritalin) in 2010 for every one person who used them in 2001

100
Percent increase in the number of  children under age 10 taking antipsychotic medications

40
Percent increase in the number of girls being prescribed ADHD medications

23
Percent of people in the “diabetes belt” states of Tennessee, Kentucky, Mississippi, and Alabama who are on at least one psychiatric drug, according to the AP

Sources: Associated PressDaily BeastHuffington Post, LA Times

http://theweek.com/article/index/221575/americas-startling-use-of-mental-illness-drugs-by-the-numbers

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Psychiatry fighting over what is and what isn’t a mental disorder…again

Thursday, November 17th, 2011
Note from CCHR: We modified the original headline (below) for the sake of accuracy.
Expanding catalog of mental disorders worries some anyone who is rational

Networks – November 16, 2011 by Maiken Scott

The so-called bible of psychiatry, the Diagnostic and Statistical Manual of Mental Disorders, is getting a make-over. The latest version, DSM 5, will come out in 2013. In the meantime, conflicts over which diagnoses should be added, removed or changed are heating up.

Thousands of mental health professionals who are not happy with the direction of the new DSM are signing an online petition.

The DSM is a highly influential publication—it guides diagnosis, research and policy. The last edition of the manual was published in 1994, meaning this new edition must reflect almost 20 years of new research and treatment advances. The stakes are high, and so is anxiety around changes and additions.

The online petition posted by several professional organizations for psychologists criticizes those working on the new DSM for what they call “lowering diagnostic thresholds.”

Philadelphia psychologist Cindy Baum-Baicker, who has signed the petition, said the number of different mental health diagnoses is growing too quickly.

“We already have 297 diagnoses. When we started the DSM, we had 106,” she said. “We’re going to have even more.”

She is concerned about several specific aspects of the new DSM, for example changes that could turn prolonged grieving into a diagnosis. Grief, she said, is a natural and important part of life.

“If we pathologize the sadness of grief, and we put people on medicine so that they don’t experience their sadness and feel it through, they oftentimes aren’t going to be making the changes they need to be making to get on with life,” Baum-Baicker said.

University of Pennsylvania psychology professor Marna Barrett has not signed the petition—even though she shares some of the concerns it addresses.

She said the professionals working on the DSM have been receptive to feedback—which she says is a good thing, but can also cause difficulties.

“In no other aspect of medicine do we have a handbook of disorders where the public can put their two cents in as to what is a disorder or not, where colleagues can say this is a disorder or not,” Barrett said.

Barrett said decisions about the DSM should be firmly based in evidence and research and not yield to social and political pressures, or lobbying efforts from interest groups such as advocacy organizations headed by parents or consumers.

The online petition criticizing the DSM has collected more than 6,000 signatures so far.

 

 


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How PTSD took over America

Wednesday, November 16th, 2011

Salon Magazine- November 15, 2011 by Alice Karekezi

The diagnosis is now being applied to everything from muggings to childbirth. An expert explains why it’s bad news

We’re not saying that people don’t have difficult emotional experiences and aren’t suffering. What we’re saying is this is not necessarily a disorder that people are experiencing, and if people think like that, it can be very disempowering to them. ( Photo Credit: David Royal Hanson via Shutterstock)

In the past 30 years, post-traumatic stress disorder has gone from exotic rarity to omnipresent. Once chiefly applied to wartime veterans returning from combat, it is now a much more common diagnosis, still linked to traumatic events but now including those occurring outside the battle zone: the death of a loved one on a hospital bed, a car crash on the highway, an assault in the neighborhood park. Many would argue that this is a good thing: greater recognition of psychologically distressing events will lead to more people seeking treatment and a decrease in the preponderance of PTSD – a win-win.

Stephen Joseph disagrees. In his new book, “What Doesn’t Kill Us,” the professor of psychology, health and social care at the University of Nottingham (in the U.K.) warns that our culture’s acceptance of PTSD has become excessive and has led to an over-medicalization of experiences that should be considered part of ordinary, normal, human experience. This has kept us from proactively working through our grief and anxiety: We’ve become too quick to go to the shrink expecting him to fix us, rather than allowing ourselves the opportunity to grow and find new meaning in our lives as a result of painful, but common, events. Joseph advocates for a push toward post-traumatic growth as therapy to treat the stress of trauma, which he distinguishes as being different from the hokey, blue skies and rainbows, pop psychology that he claims has exploded in our culture in the past decade.

Joseph spoke to Salon over the phone to discuss our misunderstanding of the disorders, the meaning and usefulness of suffering, and if some cultures are more prone to PTSD than others.

How would you define a traumatic event? Is it subjective or are there some basic requirements that must be met?

I see trauma as a psychological rupturing. It’s when something happens to us that ruptures our psychological skin. Or, something which shatters our assumptions about ourselves in the world. That’s what I think of as traumatic, and in a way that can be many things. So, that can include a wider range of experience, and I can understand trauma in that broader way. There are lots of different experiences, such as being in a road traffic collision, or experiencing an illness – those sorts of things can be traumatic to people. It can be experienced as psychologically traumatic. But whether it’s necessary to create a psychiatric diagnostic category to capture those experiences is perhaps not necessary.

Do you believe that PTSD is over-diagnosed?

Well, that’s a really, really tricky question to answer because in a way it’s diagnosed pretty much exactly as it’s described in the Diagnostic and Statistical Manual (DSM). So whether the definition of PTSD is too broad is a different question, if you see what I mean. When PTSD was first introduced in 1980, it was defined much more tightly. The gatekeeper criterion to the diagnosis was: Have you experienced a traumatic event? In 1980, it was defined in such a way that only people who had experienced an event that was really outside the range of usual human experience, [like] Vietnam or the Holocaust, had experienced the sorts of experiences that were thought to elicit PTSD. So if you experienced something like a car accident or a traumatic birth, then you couldn’t get a diagnosis of PTSD, because, by definition, you hadn’t experienced a traumatic event.

In 1994, the definition changed in such a way as to include other, broader experiences. Equally persistent was the person’s subjective experiences of what they thought was traumatic. When that happened, people who had experienced car accidents, traumatic births, what we would have otherwise thought of as more ordinary life events, insofar as they are not statistically unusual, could then be diagnosed as a having PTSD. So now we are in a position where lots of people are able to receive the diagnosis of PTSD. So it’s not that it’s being over-diagnosed in that sense. The difficulty or problem, if there is one, is whether, generally speaking – PTSD would be part of this – the DSM over-medicalizes human experience. Things which are relatively common, relatively normal, are turned into psychiatric disorders.

Can you describe some of the typical symptoms of PTSD?

When people experience trauma, when their assumptions about themselves and the world come crashing down, there’s often a period of avoidance. People just try to block out what happened. Switch off. Turn their attention to other things. That’s quite understandable. Then, over time, that gives rise to memories and emotions that come flooding in as the person sort of begins to try to make sense of what happened, and that can become so powerful and distressing that they have to push that away again and go back into a period of avoidance. So sometimes people go through that, periods of avoidance and intrusion. That seems to me as a healthy and adaptive way of working through something painful, emotionally painful, that has happened to us. So those are the experiences. PTSD is when those experiences become so overwhelming that the person can’t function anymore – at work, or school, or in their social life. It takes over so much. But otherwise the symptoms of PTSD are fairly normal, natural ways of dealing with adaptation.

It’s important to see those experiences as quite normal and natural. They are not symptoms of a disorder by themselves. They’re just the way that people deal with an upsetting event in order to be able to make sense of things and to move on. It’s only when they become so overwhelmingly intense that they might be considered a disorder. I think that’s where we get into the problem with what PTSD is: when people are going through that normal experience, but they see it as having a disorder rather than a normal process of adaptation.

That will diminish over time?

Exactly.

Is the emotional pain overblown in such cases?

The suffering is very real. We’re not saying that people don’t have difficult emotional experiences and aren’t suffering. What we’re saying is this is not necessarily a disorder that people are experiencing, and if people think like that, it can be very disempowering to them.

What is the detrimental effect of over-medicalizing these more common human experiences of grief and pain?

When we think of ourselves as suffering from a disorder in a medical sense, well we go to the doctor and we expect the doctor to prescribe whatever the medical treatment is. We’re not in the driver’s seat. We go along – we tell them [our] symptoms, they listen to us, they diagnose what the problem is, and then they work out what the appropriate treatment is. That’s the mind-set when we’re working within a medical framework and we think of ourselves as suffering from a disorder. We sit down in front of the therapist and we expect the therapist to be like a doctor – to be looking out for what the symptoms are so that they can make the correct diagnosis and prescribe us the right treatment. The language of PTSD invokes those ideas, and I think it’s those ideas that can be quite unhelpful at times. For what we’re talking about here, if it’s a normal, natural process, what’s really important is for the person to be in the driver’s seat for themselves – to make their own choices, their own decisions, because we’re dealing not with a disorder, but a battle within the person to find new meanings and new ways of understanding the world. That’s what they have to do. Nobody else can do that for them.

What is “post-traumatic growth”?

Post-traumatic growth is when people come out of trauma having learned new things about themselves and about the world and about their relationship with the world. People develop new philosophies of life. They develop new priorities in life. People learn an awful lot about themselves: their strengths; what they’re good at; having new respect for themselves. They sort of see their lives as divided into two halves: before the event happened and after the event happened. There is a clear demarcation. And they recognize that something happened to them that sliced their world in half in that way, and things for them are now completely different. How they lead their lives has been transformed – their priorities about life, their relationships.

I think one of the things that captures that the most [starts with] the idea that, sometimes, people lead their lives in a way that is dictated by external forces of status and wealth, which are very much big drivers in our capitalist society. We often, in our everyday lives, forget about the small things that are quite important – our relationships: remembering to nurture them, to look after the people around us, to be giving, to be compassionate. When traumatic events happen, people are often shaken back to reality, and remember what really matters to them. Often it is those other things – remembering somebody’s birthday; nurturing our friendships; looking after our parents, the people around us; really embracing our relationships; and letting go of a more materialistic outlook. People often describe it as getting back to who they really are, or feeling more true to themselves, or being more genuine or more authentic. Somehow the idea of the false self that people create around them is shattered, like Humpty Dumpty falling off a wall. The essence of who they are emerges.

Yes, becoming truer to oneself captures the idea very well. Realizing that life is short and sometimes there isn’t as much time left as we thought to put up facades.

This kind of makes trauma sound like a blessing (you even mention people describing it as a “gift”). Is finding meaning the same thing as condoning the traumatic event? And doesn’t this talk of growth all sound very “kumbaya-ish” and unrealistic?

One of the reasons, sometimes, that post-traumatic growth can be seen unfavorably is that it seems like saying that trauma can lead to greater happiness; that for people who have been through trauma, it’s a good for them – they’re happier. That’s just so not the message. It’s not saying that trauma leads to happiness, in terms of smiling and feeling good and laughing and joy – not that type of happiness. What we’re talking about is how trauma can lead to a deeper, more existentially meaningful and fulfilling life, and that in turn may lead to greater happiness further down the road. But, post-traumatic growth is not about happiness in the sort of yellow, smiley face sense.

In essence, post-traumatic growth is a very simple idea, but it has been overshadowed by this mass of psychiatric literature over the past 30 or 40 years about the overwhelming destructive side of trauma, and about how these lead to medical problems. It’s a very simple idea, but [post-traumatic growth] sits, on the one hand, very uncomfortably within mainstream culture of the world of psychology and psychiatry, and on the other hand it seems to sit very comfortably with some other parts of Western culture, such as positive thinking, but it also clashes with some of that literature which is quite superficial, and not grounded in scientific research, and makes unsupported claims.

So, no, post-traumatic growth] doesn’t mean that [people] value or cherish the bad thing that has happened to them. They just accept that it has happened to them. People will often say they wish it hadn’t happened, or they wish they could go back, but there is a realism that they know they can’t. So it’s accepting that they can’t go back; they can’t change things. The only way forward is to go forward. It’s when people can’t accept that something has happened, and they [try] to go back to how they were before, is when they struggle. Acceptance is just being realistic – not seeing it as a good thing.

And someone not experiencing growth — or experiencing PTSD — is that person always trying to go back?

I think that often that’s what gets people stuck – trying to go back, trying to rebuild their lives exactly as it was before. That can lead people to get very stuck because it just isn’t possible when traumatic events happen and we’re presented with new information about the world, or with losses. It just isn’t possible to go back and make things as they were. We have to somehow accept what has happened to us and move on.

Is post-traumatic growth something completely in opposition to PTSD or post-traumatic stress? Either you have one or the other?

They can sit together. The way I see it, post-traumatic growth mostly arises out of post-traumatic stress. So it’s how people deal with the post-traumatic stress; how they manage to deal with the intrusive thoughts that are plaguing them; and the new sense they make of their experiences. So it’s through the post-traumatic stress, through the struggle of post-traumatic stress that post-traumatic growth arises. So often there’s a period of time in which people will begin to talk about post-traumatic growth but they will still be suffering from post-traumatic stress. They’re not in opposition. In a way, they are opposite sides of a coin.

You make a claim that true happiness is something that in and of itself cannot be pursued, and one is doomed to fail if one tries. How is that?

Well, that’s an idea that some philosophers have put forward. Some of the research seems to suggest that what’s really important to finding happiness is meaning and purpose in life. If we think our road to happiness is through seeking hedonistic pleasures night after night, then that’s not likely to lead to a deep, fulfilling level of happiness. But, if we find ways of finding meaning and purpose, wherever that might be, then we’re not setting out directly aiming for happiness but that’s what we’re going to get. We’re going to find a more fulfilling life. Happiness is a byproduct, but in a sense it’s more guaranteed.

When we think of psychological therapies, and the helping professions in general, they often have been about helping people feel better. [For] people with various problems of depression, anxiety or post-traumatic stress, therapy is about getting the person to have a more positive emotional state. That’s been, really, what the therapy world has been about for 50 years, and yet that’s only half the picture. The other half is about the meaning we put on things, our purpose in life, our sense of ourselves, our sense of autonomy, our relationships. Psychology can also be about those things. I’m not saying that therapists have ignored them altogether; for sure, they haven’t, but those more existential ideas have been overshadowed by trying to feel good. This is the idea between what psychologists call subjective well-being, which is about feeling good, and psychological well-being, which is what you could call “meaning-good,” and it’s just about getting the balance between those two things right.

Are there some cultures that are more prone to post-traumatic growth?

That’s a really good question. I don’t think the research has really documented that yet as to whether it may be more common. What the research has shown, however, is that post-traumatic growth is something observed in pretty much all cultures that have been investigated, though differently defined in slight ways. “Post-traumatic growth” sounds like a very Western idea, but [it’s one that] gets back into history and into all sorts of cultures. It’s an idea that’s very resonant with Buddhist and some Chinese philosophy ideas, as well as ideas in Western religion.

http://www.salon.com/2011/11/15/how_ptsd_took_over_america/singleton/

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Canadian Kids are All on Drugs

Tuesday, November 15th, 2011

The Mark – November 14, 2011

Kids as young as six are being prescribed powerful antipsychotic drugs

The number of prescriptions for antipsychotic drugs for kids in Canada more than doubled between 2005 and 2010. A study in the journal Pediatrics & Child Health shows that the number of prescriptions jumped 114 per cent across those years, despite most antipsychotics not being cleared for use in Canada among people younger than 17. The drugs are used to offset the symptoms of attention deficit hyperactive disorder, autism, mood disorders, and all manner of behavioural problems in kids as young as six. According to Postmedia‘s Sharon Kirkey and Pamela Fayerman:

Once reserved for schizophrenia and mania in adults, one antipsychotic alone, risperidone, was recommended by Canadian-office-based doctors for children 17 and younger a total of 340,670 times in 2010 – a near-doubling since 2006 – according to data provided to Postmedia News from prescription-drug tracking firm IMS Brogan.

Not too surprisingly, the level of prescriptions has some doctors wondering if these drugs are being overprescribed. Complicating matters are the side effects of the drugs, which can lead to rapid weight gain, pre-diabetes, obesity, tremors, and more. Likewise, long-term studies on the drugs’ effects on kids’ health aren’t readily available.

Get the facts about antipsychotic drugs here

http://www.themarknews.com/news/?open=7441

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Addiction Specialist Says It’s Easier to Withdraw Patients from Heroin than from Xanax

Monday, November 14th, 2011

KNTV – November 14, 2011

"It's so much easier to take people off heroin. I'd rather take 100 people off heroin than one person of Xanax because I know they'll have a year of withdrawal," says addiction specialist Dr. Jerry Callaway.

Also known as Alprazolam, it’s the 11th most prescribed drug in the United States, but you often don’t need a doctor to get it.

22-year-old “Nick” is a recovering Xanax addict.

In addition to getting them at parties, he says he also would get prescriptions for hundreds of Xanax pills from doctors.

“All you have to do is walk into a doctor’s office and say you have anxiety, at least that’s what I did and it was written to me,” he says.

Nick says he knew he had to kick the drug when he took Xanax, blacked out while driving and seriously injured three people.

“It’s sobering to know my actions caused innocent people great bodily injury,” he now says.

Doctors warn weaning off the drug has serious risks too.

“It’s so much easier to take people off heroin. I’d rather take 100 people off heroin than one person of Xanax because I know they’ll have a year of withdrawal,” says addiction specialist Dr. Jerry Callaway.

A spokeswoman for Pfizer, the manufacturer of Xanax says, “When prescribed and taken as indicated Xanax has a well established safety profile and is an important treatment option that has benefitted millions of patients.”

Between 2004 and 2008 the Centers for Disease Control reported an 89 percent increase in the number of emergency room visits nationwide related to the non-medical use of Xanax and other drugs in its class.

According to drug site which reviews the FDA’s adverse events data base, people using Xanax reported more than 11,000 adverse events between 2004 and march of this year.

They include 83 deaths, 107 completed suicides and 100 comas.

Addiction experts also say you might be surprised whose abusing Xanax.

“It might be a stay-at-home mom or a working mom, and in an attempt deal with the overwhelm of that they go to the doctor, they talk to them about the anxiety, they talk about the overwhelm the doctor prescribes them Xanax and next thing you know now they’re addicted to it,” says treatment center director Lori Johnson.

The FDA does require a warning to patients that Xanax can become addictive, but there is a petition asking them to add a stronger and more visible safety alert.

“I think it’s overdue,” Dr. Callaway says.

Nick, who has now gone six months without Xanax, has a warning of his own for those considering experimenting with the drug.

“At all costs stay away from it. There’s nothing good about it, nothing good can come out of Xanax,” he says.

http://www.ksdk.com/news/article/285646/9/Xanax-building-dangerous-reputation

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Nazi Eugenics Employed — in North Carolina

Thursday, November 10th, 2011

“Between 1929 and 1974, the state – through its North Carolina Eugenics Board – authorized sterilizations of about 7,600 North Carolina residents classified as mentally ill, epileptic or “feeble-minded,” which generally meant an IQ of less than 70, the Observer said.“  — North Carolina Observer, November 10, 2011  (read the rest of the article below our note)

Note from CCHR on Eugenics:  In 1869,  English psychologist Francis Galton created the word “eugenics” from the Greek word, eugenes, meaning “good stock.”  He encouraged using “better” human stock from which to breed, and discouraged what he considered “less desirable” stock from having children, evidently considering himself part of the “better” stock and thereby capable of judging the future for all humanity. In 1870, British psychologist Herbert Spencer claimed that selective breeding of the fittest would bring about a superior race, while the unfit should be allowed to die out.  These notions of cultural hierarchy caught on in the United States and by the 1920s, eugenics sterilization was practiced in two-dozen states, with California accounting for more than half of the 16,000 operations performed between 1907 and 1933.  Beyond that, they formed the basis of much of Hitler’s Mein Kampf and the Holocaust that followed.

Nazi psychiatrist Ernst Rudin

In 1933 psychiatrist Ernst Rudin was chosen by Hitler’s Reich Ministry to lead Germany’s racial purity program. Rudin wasted no time in drafting the Nazi Sterilization Law which originally called for the sterilization of “schizophrenics,” “alcoholics,” and “manic-depressives” — the subjects of Rudin’s “research.” As these legal sterilizations began, programs were already underway to sterilize “black” Germans. The sterilization program expanded to include Jews, Gypsies and, in the words of Rudin, other “inferior race types.”  By the end of World War II, two million had been sterilized.  The majority of those sterilized were between the ages of twenty and forty.

Ernst Rudin praised Hitler and the Nazis for their “decisive… path-breaking step toward making racial hygiene a fact among the German people… and inhibiting the propagation of the congenitally (hereditarily) ill and inferior.”  He stated, “Only through the Fuhrer did our dream of over thirty years, that of applying racial hygiene to society, become a reality.”

 

The Post Chronicle – November 9, 2011

Force Sterilization Victims Speak Out

North Carolina officials report they have located only 41 survivors of thousands of state residents forced to undergo sterilization.

The Charlotte Observer reports state officials have spent more than a year trying to find those who had been sterilized so they can be compensated, because the operations were medically unnecessary and immoral.

Between 1929 and 1974, the state – through its N.C. Eugenics Board – authorized sterilizations of about 7,600 North Carolina residents classified as mentally ill, epileptic or “feeble-minded,” which generally meant an IQ of less than 70, the Observer said.

The newspaper said Wallace Kuralt, the head of the Mecklenburg County Welfare Department from 1945 to 1972, had a nationwide reputation as a leader in eugenic sterilization. In his words, his department sought clients from among “low mentality-low income families which tend to produce the largest number of children.”

He considered sterilization part of progressive family planning.

Some women came to the state pleading to be sterilized, particularly before the birth control pill. But Mecklenburg County advocated the operations for people who were poor, disabled or in trouble, the Observer said.

Most of the sterilizations occurred in the 1950s and early 1960s.

Today, parents can ask a judge to have a child sterilized but only as a last resort.

Ellen Russell, director of advocacy for The Arc of North Carolina, a non-profit that works with developmentally and intellectually disabled people, says IQ is not a dependable measure of someone’s ability to raise children.

“There are certainly people with developmental disabilities who can raise children well,” Russell said. “As there are people without developmental disabilities who can’t.”

In June of this year, officials heard gut-wrenching testimony from men and women sterilized by the state during a 50-year period to cut welfare costs.

The stories of about a dozen of the nearly 7,600 people who were sterilized at the direction of the state were heard during testimony before a state task force that will recommend ways to compensate them, The (Raleigh) News and Observer reported.

From the 1920s to the 1970s, the state-funded Eugenics Board determined certain groups of people – the poor, undereducated or mentally unstable – were unfit for parenthood. Former Gov. Mike Easley apologized to the state’s eugenics victims in 2002, but there has been no compensation so far.

Gov. Bev Perdue and four state representatives attended the session, thanking the victims for sharing their stories, but made no promises of compensation.

“I came here as a woman, a mama, a grandmama, and a governor of the state to say that it was wrong,” Perdue said. “I’m here to tell you how important these hearings are.”

One woman, Elaine Riddick, 57, told the panel she became pregnant when she was raped at age 14, CBS News reported. The day she delivered her son, doctors sterilized her on orders from the state.

“They said that I was feeble-minded, they said that I was promiscuous,” Riddick told CBS News. “I’ve always been able to take care of myself – I’ve never been promiscuous. So how can people use these things to describe a child that had been abandoned? Or that had been raped by the neighbor and then again, raped by the state of North Carolina?”

North Carolina state Rep. Larry Womble, a Democrat sitting on the task force, said he hoped lawmakers would pass legislation that would allow eugenics victims to receive compensation, as well as counseling and medical help.

CBS News said more than 60,000 people in 32 states were affected by state-sanctioned sterilization programs aimed at cutting welfare costs.

“The people who were the focus of this movement were the dispossessed of society,” Paul Lombardo, of Georgia State University’s College of Law, said. “In some cases, simply people of color.”

http://www.postchronicle.com/news/health/article_212389314.shtml

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Hundreds of Soldiers & Vets Dying From Antipsychotic–Seroquel

Monday, November 7th, 2011

Market Watch
November 7, 2011

Fred A. Baughman Jr., MD & Stan White (Father of Deceased Veteran, Andrew White) disclose the following:

EL CAJON, Calif., Nov. 7, 2011 /PRNewswire via COMTEX/ — As a neurologist who has discovered and described medical diseases, I (Fred A. Baughman) read the May 24, 2008, Charleston (WV) Gazette article “Vets taking Post Traumatic Stress Disorder drugs die in sleep,” and opened and financed my own investigation into these unexplained deaths.

Andrew White, Eric Layne, Nicholas Endicott and Derek Johnson, all in their twenties, were four West Virginia veterans who died in their sleep in early 2008. There were no signs of suicide or of a multi-drug “overdose” leading to coma, as claimed by the Inspector General of the VA. All had been diagnosed “PTSD”–a psychological diagnosis, not a disease (physical abnormality) of the brain. All were on the same prescribed drug cocktail, Seroquel (antipsychotic), Paxil (antidepressant) and Klonopin (benzodiazepine) and all appeared “normal” when they went to sleep.

On February 7, 2008, Surgeon General Eric B. Schoomaker, had announced there had been “a series, a sequence of deaths” in the military suggesting this was “often a consequence of the use of multiple prescription and nonprescription medicines and alcohol.”

However, the deaths of the ‘Charleston Four’ were probable sudden cardiac deaths (SCD), a sudden, pulseless condition leading to brain death in 4-5 minutes, a survival rate or 3-4%, and not allowing time for transfer to a hospital. Conversely, drug-overdose coma is protracted, allowing time for discovery, diagnosis, transport, treatment, and frequently–survival.

Antipsychotics and antidepressants alone or in combination, are known to cause SCD. Sicouri and Antzelevitch (2008) concluded: (1) “A number of antipsychotic and antidepressant drugs can increase the risk of ventricular arrhythmias and sudden cardiac death,” (2)”Antipsychotics can increase cardiac risk even at low doses whereas antidepressants do it generally at high doses or in the setting of drug combinations.”

On April 13, 2009, Baughman wrote the Office of the Surgeon General (OTSGWebPublisher@amedd.army.mil): “On February 7, 2008 the Surgeon General said there had been ‘a series, a sequence of deaths.’ Has the study of these deaths been published?”

On April 17, 2009 the Office of the Surgeon General responded, “The assessment is still pending and has not been released yet.” More than a year later and still no explanation, nor further acknowledgement that these deaths even took place.

In a press release, (PRNewswire, May 19, 2009) Baughman wrote: “I call upon the military for an immediate embargo of all antipsychotics and antidepressants until there has been a complete, wholly public, clarification of the extent and causes of this epidemic of probable sudden cardiac deaths.”

Googling “dead in bed,” “dead in barracks,” by April 16, 2009, veteran’s wife, Diane Vande Burgt, had Googled 74 probable sudden cardiac deaths. By May 2010: 128, and, by November 2, 2011: 247. Two-hundred-forty-seven!

In April 2010 I was in anonymous receipt of an Army National Guard Serious Incident Report for the 5 months 10/03/09 to 3/7/10. In it were 93 “incidents” including 4 “heart attacks,” 6 “cardiac arrests” and 3 “found dead”; 13 of 93 (14%) probable SCDs.

Pfc. Ryan Alderman, was on a cocktail of psych drugs when found unresponsive, dying in his barracks at Ft. Carson, Colo. Sudden cardiac death was confirmed by an ECG done at the scene. Inexplicably, military officials de-classified his death and reversed the cause, calling it instead, a “suicide.”

Again I challenge the military to produce the evidence.

In June 2011, a DoD Health Advisory Group backed a highly questionable policy of “polypharmacy” asserting: “…multiple psychotropic meds may be appropriate in select individuals.” The fact of the matter is that psychotropic drug polypharmacy is never safe, scientific, or medically justifiable. What it is a means of (1) maximizing profit, and (2) making it difficult to impossible to blame adverse effects on any one drug.

From 2001 to the present, US Central Command has given deploying troops 180 day supplies of prescription psychotropic drugs–Seroquel included. In a May 2010 report of its Pain Management Task Force, the Army endorsed Seroquel in 25- or 50-milligram doses as a ‘sleep aid.’

Over the past decade, $717 million was spent for Risperdal and $846 million for Seroquel, for a mind-blowing total of $1.5 billion when neither Risperdal nor Seroquel have been proven safe or effective for PTSD or sleep disorders.

Ironically, yet not surprisingly, pay-to-play in Washington becomes more egregious every day. Heather Bresch, daughter of U.S. Sen. Joe Manchin, (D-WV) was recently named CEO of WV drug-maker Mylan Inc., that recently contracted with the DoD for over 20 million doses of Seroquel.

Defense Department Health Advisory Group chair, Charles Fogelman, warned: “DoD currently lacks a unified pharmacy database that reflects medication use across pre-deployment, deployment and post-deployment settings.” In essence, through a premeditated lack of record keeping, mandated by law at any other pharmacy or medical office to track potential fatal reactions to mixing prescription drugs, the military is willfully preempting all investigations into the injuries and deaths due to psychiatric drugs.

I call on the DoD, VA, House and Senate Armed Services and House and Senate Veterans Affairs Committees to tell concerned Americans and the families of fallen heroes what psychiatric drugs each of the deceased, both combat and non-combat, soldiers and veterans were on?

It is time for the military and government to come clean.

http://www.marketwatch.com/story/hundreds-of-soldiers-vets-dying-from-antipsychotic-seroquel-2011-11-07

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Fraud Case Seen as a Red Flag for Psychology Research

Monday, November 7th, 2011

The New York Times
By Benedict Carey
November 2, 2011

The psychologist Diederik Stapel in an undated photograph. "I have failed as a scientist and researcher," he said in a statement after a committee found problems in dozens of his papers. (Photo: Joris Buijs/Pve)

A well-known psychologist in the Netherlands whose work has been published widely in professional journals falsified data and made up entire experiments, an investigating committee has found. Experts say the case exposes deep flaws in the way science is done in a field, psychology, that has only recently earned a fragile respectability.

The psychologist, Diederik Stapel, of Tilburg University, committed academic fraud in “several dozen” published papers, many accepted in respected journals and reported in the news media, according to a report released on Monday by the three Dutch institutions where he has worked: the University of Groningen, the University of Amsterdam, and Tilburg. The journal Science, which published one of Dr. Stapel’s papers in April, posted an “editorial expression of concern” about the research online on Tuesday.

The scandal, involving about a decade of work, is the latest in a string of embarrassments in a field that critics and statisticians say badly needs to overhaul how it treats research results. In recent years, psychologists have reported a raft of findings on race biases, brain imaging and even extrasensory perception that have not stood up to scrutiny. Outright fraud may be rare, these experts say, but they contend that Dr. Stapel took advantage of a system that allows researchers to operate in near secrecy and massage data to find what they want to find, without much fear of being challenged.

“The big problem is that the culture is such that researchers spin their work in a way that tells a prettier story than what they really found,” said Jonathan Schooler, a psychologist at the University of California, Santa Barbara. “It’s almost like everyone is on steroids, and to compete you have to take steroids as well.”

In a prolific career, Dr. Stapel published papers on the effect of power on hypocrisy, on racial stereotyping and on how advertisements affect how people view themselves. Many of his findings appeared in newspapers around the world, including The New York Times, which reported in December on his study about advertising and identity.

In a statement posted Monday on Tilburg University’s Web site, Dr. Stapel apologized to his colleagues. “I have failed as a scientist and researcher,” it read, in part. “I feel ashamed for it and have great regret.”

More than a dozen doctoral theses that he oversaw are also questionable, the investigators concluded, after interviewing former students, co-authors and colleagues. Dr. Stapel has published about 150 papers, many of which, like the advertising study, seem devised to make a splash in the media. The study published in Science this year claimed that white people became more likely to “stereotype and discriminate” against black people when they were in a messy environment, versus an organized one. Another study, published in 2009, claimed that people judged job applicants as more competent if they had a male voice. The investigating committee did not post a list of papers that it had found fraudulent.

Dr. Stapel was able to operate for so long, the committee said, in large measure because he was “lord of the data,” the only person who saw the experimental evidence that had been gathered (or fabricated). This is a widespread problem in psychology, said Jelte M. Wicherts, a psychologist at the University of Amsterdam. In a recent survey, two-thirds of Dutch research psychologists said they did not make their raw data available for other researchers to see. “This is in violation of ethical rules established in the field,” Dr. Wicherts said.

In a survey of more than 2,000 American psychologists scheduled to be published this year, Leslie John of Harvard Business School and two colleagues found that 70 percent had acknowledged, anonymously, to cutting some corners in reporting data. About a third said they had reported an unexpected finding as predicted from the start, and about 1 percent admitted to falsifying data.

Also common is a self-serving statistical sloppiness. In an analysis published this year, Dr. Wicherts and Marjan Bakker, also at the University of Amsterdam, searched a random sample of 281 psychology papers for statistical errors. They found that about half of the papers in high-end journals contained some statistical error, and that about 15 percent of all papers had at least one error that changed a reported finding — almost always in opposition to the authors’ hypothesis.

The American Psychological Association, the field’s largest and most influential publisher of results, “is very concerned about scientific ethics and having only reliable and valid research findings within the literature,” said Kim I. Mills, a spokeswoman. “We will move to retract any invalid research as such articles are clearly identified.”

Researchers in psychology are certainly aware of the issue. In recent years, some have mocked studies showing correlations between activity on brain images and personality measures as “voodoo” science, and a controversy over statistics erupted in January after The Journal of Personality and Social Psychology accepted a paper purporting to show evidence of extrasensory perception. In cases like these, the authors being challenged are often reluctant to share their raw data. But an analysis of 49 studies appearing Wednesday in the journal PLoS One, by Dr. Wicherts, Dr. Bakker and Dylan Molenaar, found that the more reluctant that scientists were to share their data, the more likely that evidence contradicted their reported findings.

“We know the general tendency of humans to draw the conclusions they want to draw — there’s a different threshold,” said Joseph P. Simmons, a psychologist at the University of Pennsylvania’s Wharton School. “With findings we want to see, we ask, ‘Can I believe this?’ With those we don’t, we ask, ‘Must I believe this?’ ”

But reviewers working for psychology journals rarely take this into account in any rigorous way. Neither do they typically ask to see the original data. While many psychologists shade and spin, Dr. Stapel went ahead and drew any conclusion he wanted.

“We have the technology to share data and publish our initial hypotheses, and now’s the time,” Dr. Schooler said. “It would clean up the field’s act in a very big way.”

http://www.nytimes.com/2011/11/03/health/research/noted-dutch-psychologist-stapel-accused-of-research-fraud.html?_r=1

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