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After finishing Jeffrey Lieberman’s new book, Shrinks: The Untold Story of Psychiatry, I was tempted to put it aside and not write anything, even though I had purchased the book with the intention of doing so. The reason was that I found it impossible to take the book seriously, and actually, I don’t think it is meant to be a serious book. But eventually it dawned on me: The revelatory aspect of Shrinks is that it serves as an institutional self-portrait. What you hear in this book is the story that the APA and its leaders have been telling to themselves for some time.

Since the 1980s, a type of psychotherapy called Cognitive Behavioural Therapy (CBT) has become dominant. Like it or loathe it, CBT is now so ubiquitous it is often the only talking therapy available in both public and voluntary health settings. It is increasingly spoken about in the media and in living rooms across the country. Yet when we speak about CBT, what are we talking of? For CBT only exists - as we will see - as a political convenience.

I have some trepidation as a social worker venturing into the world of ecology and biodiversity but during my recent visit to Hawaii, I began to realize there are some parallels in that world and ours. Could psychiatric medications be considered an invasive species in the world of mental health?

Somewhere along the line we have lost the understanding that kids come in all shapes and sizes. Some kids are active, some are quiet; some kids are dreamers, others are daring; some kids are dramatic, others are observers; some impulsive, others reserved; some leaders, others followers; some athletic, others thinkers. Where did we ever get the notion that kids should all be one way?

My law review article entitled "Rethinking criminal responsibility from a critical disability perspective: The abolition of insanity/incapacity acquittals and unfitness to plead, and beyond" has been published in Griffith Law Review. The article attempts to find a way to deal with concerns for a degree of toleration towards socially disruptive behavior that may be criminalized, without making some people categorically and legally irresponsible as happens with the insanity defense.

The American Psychological Association (APA) recently released its annual 2015 Stress in America survey.  For the 9^th straight year (since the survey began), financial issues were reported as the number one stressor in America.  Even while many parts of the U.S. economy have shown a resurgence, many Americans are reporting that financial strain continues to take its toll, likely having significant effects on our health and well-being.

It's no secret that here in America, foster children are being prescribed psychiatric drugs, especially neuroleptics, as a means of controlling their behavior. A great deal has been said and written on the matter. Politicians have declared the practice deplorable. Children's advocacy groups have expressed concern, and, of course, those of us in the antipsychiatry movement have screamed till we're hoarse. But the problem persists.

This is the second of a series of excerpts from Cracked Open, a book whose unintentional beginning came after I became physically dependent on Ativan in 2010. After a year of following my doctor’s orders for daily use to treat insomnia, my body and mind began to fall apart. I’m serializing the book here – before sending it out into the world – because MIA became a lighthouse for me. I want this community’s feedback because I want to help make a difference. I want my words and message to be clear and strong.

I learned of the Hiawatha Asylum for Insane Indians in 2001 through the paper, “Wild Indians,” by psychiatric survivor and activist Pemina Yellow Bird. Pemina movingly described the notorious history of this federal facility which operated from 1899 to 1933. When I finished reading, I searched up Pemina’s email address, and we began a series of lengthy virtual exchanges that helped galvanize my spirit through the many emerging battles with IHS’s psychiatric labeling and medicating approach to treating Yakama reactions to oppression, and the related psychosocial stress. In short, I began to fight back.

Being a woman of a certain age, I dutifully went in for a “routine” colonoscopy a few weeks ago. My doctor came to see me before the procedure. She spent about 5 minutes reviewing the procedure and asked me to sign the consent form. I was in the procedure room for about 10 minutes and then we were done. A few days ago, I got the bill. It got me to wondering about the reimbursement for the work I do.

I read some Hegel in a reading group a few years ago and was bowled over by it. So I was excited to find a book that analyses Hegel’s ideas about the nature of madness, and wanted to review it even though it was written 20 years ago. Hegel may not have been the first to have made this point, but for me his writing brings home, more clearly than any other thinker, the intrinsically social nature of human thought and existence.

Emergency Rooms have become the triaged door to mental health care. Even without so many walk-ins, doctors and health care workers agree that the ER may be good for heart attacks and gun shot wounds, but not for delusions, extreme agitation or despair. But if all you have is an Asylum Fix, then every worried or grieving or traumatized or elated individual looks like he or she needs long-term care. Here are 10 alternatives to crisis and misery.

I am proud and happy to announce that our webpage DrivingUsCrazy was launched today. It will help us to get the word out about the international film festival taking place in Gothenburg, 16-18 October, 2015, and also to highlight the issue of madness every day until then — and hopefully for many days afterwards.

We need all of our voices to come together to challenge that sort of power in order to have any sort of hope at all. To the best of my knowledge, the majority of people who hang around these ‘Mad in America’ parts are particularly interested in prioritizing, promoting, and creating access to (true) alternatives, including those built upon peer-to-peer supports. But, whenever one of us falls, it becomes that much easier to knock the next one down. We need more examples to point to, not less; more places to reference and say, “If they can do it, why can’t we?”; more places to call upon and say, “If you don’t believe us, how about them… or them… or them?”

Those of you who read the New York Times may have seen its coverage of the British Psychological Society’s recent report, ‘Understanding Psychosis and Schizophrenia: Why people sometimes hear voices, believe things that others find strange, or appear out of touch with reality, and what can help.’ The report has been widely welcomed and many have seen it as a marker of how our understanding of these experiences is changing. The report has not been without its critics. We (Editor Anne Cooke and co-author Peter Kinderman) are coming to New York this month to launch the report in America.

When I started my practice as a child therapist in 1988, I had barely heard of attention-deficit/hyperactivity disorder or ADHD. The diagnosis had arrived on the scene a year earlier, in the revised third edition of the Diagnostic and Statistical Manual of Mental disorders (DSM-III-R). Despite its codification in the DSM, at the time ADHD was not widely discussed among child therapists, let alone parents, teachers and pediatricians. Until the middle of the 1990’s, not one mother or father asked me if their child had ADD or ADHD. By 2012, things had radically changed.

I’ve spent much of my professional life studying psychological aspects of mental health problems. Inevitably, this has also meant discussing the role of biology. That’s my academic day-job. But it’s not just academic for me. I’m probably not untypical of most people reading this; I can see clear examples of how my experiences may have affected my own mental health, but I can also see reasons to suspect biological, heritable, traits. As in all aspects of human behaviour, both nature and nurture are involved and they have been intimately entwined in a complex interactive dance throughout my childhood and adult life.

On Saturday May 16, 2015, there will be demonstrations protesting shock treatment in many cities around the world. This will be a historic event for our movement for human rights in psychiatry. I don’t know of any other time our movement has carried out such a coordinated action on this scale.

Academia has long been the official search engine for knowledge. Here supposedly are the ivory towers where seekers after truth, men and women intellectuals, teach new generations and carry out learned research, to add to the sum of human wisdom. It also has a longstanding history of questionable relationships; from those with the arms trade, to continuing over-reliance on big pharma psychiatric research funding.

Instead of hope and enthusiasm for their futures, too many children now grow up believing they are inherently defective, and controlled by bad genes and biochemical imbalances. They are shackled by the idea that they have ADHD and then subdued by the drugs that inevitably go along with the diagnosis. Unless something intervenes, many of them will go on to pass their days on Earth in a drug-impaired, demoralized state.

Mad in America has featured an article about inflammation and the immune response in the Lancet. It’s great that these things are being studied, but as usual it’s done from a dangerously reductionistic perspective. We must broaden our lenses if we hope to profoundly help people. Again, my favorite meme: everything matters.

Many psychiatric survivors have created a gift economy of sorts in offering peer support, and this is by no means to criticize those offering their best guidance freely to those who desperately need it. In fact, the gift economy saved my life when it was threatened by psychiatric drugs. Yet, my entrepreneurial spirit, as chaotic and unsophisticated as it has been at times, has played a huge role in saving me from being a chronic mental patient with a chronic identity of “sick” or “failure” or “other”.

There are no set rules for grief. It takes however long it takes, sometimes years, sometimes more. Grieving operates on its own time. The very idea that the DSM-5 gives a two-week grace period before diagnosing a ‘biological depression’ is obscene on the face of it, never mind the handing out of Prozac. Other psychiatrists would like to push the window all the way to three or even four weeks. How compassionate. There is no place for antidepressants, ever

Those of us who are concerned about the state of the behavioral health service system would agree that voluntary, cost-effective services and supports that preclude the need for coerced or institutional treatment should be widely available. Peer respites may be one component of such a system.

As I have various discussions about mental health and disability on the internet, I am disturbed at how many people continue to use the terms “high functioning” and “low functioning” when referring to people with psychiatric or other disabilities. I have heard people refer to their family members as “low functioning.” I have seen these terms used by advocates to bully and discredit other advocates who critique calls for increased levels of involuntary treatment as “high functioning” individuals who don’t know what they’re talking about.