Hothouse flowers

A mesmerizing story about Japan’s Chrysanthemum Throne hothouse appears today in the New York Times. As uniquely Japanese as the tale appears, what lies beneath is universal. Crown Princess Masako, who suffers from depression and is not often seen in public, now appears to have a daughter who may be showing early signs of nervousness.

Then there is the Washington Post story about Patrick Kennedy not seeking re-election for a ninth term. I give him credit for weathering the storm of the public eye for sixteen years despite having familial tendencies toward drink and manic-depression.

Kennedy says he intends to work for mental health and addiction issues from his home base of Portsmouth, Rhode Island. “As exciting and as meaningful as work is and as my career is, ultimately something clicked inside of me that there was something that was missing,” Kennedy says. “I want a fuller life.”

I wish him the best of luck. I can guarantee him a fuller life if he, for personal and professional reasons, decides to investigate the healing world of holistic mental health. He can also develop a reading list of the great inner life authors – Hermann Hesse, Kierkegaard, Neitsche, to name just a few. The Big Bang and energy medicine should be on the reading list, too. We are put here on earth to do more than simply cope with our problems. We can transform them.

“We grew up in a family where there was very little tolerance for self-exploration,” says a cousin, Christopher Kennedy Lawford. “I think now he has this freedom . . . to do some real exploration of who he is and what he wants to do in his lifetime. That’s a valiant exploration, and a needed one.

“Gandhi,” he adds, “said the man who conquers himself is greater than the man who conquers 10,000 armies.”

Orgone energy

Actor Orson Bean’s book, Me and the Orgone, about his experiences with orgone therapy under Dr. Elsworth Baker, is an interesting look at a little known therapy. My one disappointment with the book is that his therapy didn’t involve the use of the orgone accumulator box that was so popular with beat generation writers and poets. According to J.D. Salinger’s daughter, he used to sit for days at a stretch in the accumulator and drink his own urine. (Daughter obviously had “issues” with dear old Dad.)

Orgone therapy involves circulating the natural flow of energy around the body by pushing and pounding and pinching various places in the body to loosen the bodily armour (defense mechanisms) that build up due to life’s traumas and layer like scar tissue. The body adapts, but is locked.

The trauma that Orson’s Bean confided to in the book was how badly he felt when his parents got rid of his dog when he was about ten and that he never cried when his mother died. It was also obvious that he felt unfulfilled sexually and that was largely the reason behind his entering into orgone therapy. Three and a half years of orgone therapy once a week accomplished more than what ten years of psychoanalysis did for him. He felt released.

Orgone therapy involves the manipulation of what has come to be called putative (non-measurable) energy or chi. It can be consider a category of energy medicine and is cathartic in nature.

See also Psychiatric home remedies.

The relapse double standard

Trolling the Internet today for inspiration, here’s yet another example of what I consider a double standard for how differently schizophrenia is viewed from other mental health issues when it comes to relapse. When someone with a diagnosis of schizophrenia relapses, cries go out that is is due to going off the drugs, which “everybody knows” someone with schizophrenia cannot do.

My point has always been that people will relapse if they haven’t effectively dealt with their problems. Yes, I know it is also true that the drugs create problems so that withdrawing from them can lead to re-emergence of the symptoms, but that’s not the point here I am making. Isn’t it time that doctors attribute relapse in schizophrenia to the same reasons alcoholics, sex addicts or depressed people relapse?

Based on the addiction model, several sex addiction treatment centers have opened in recent years — including Pine Grove in Hattiesburg, Miss., where rumors have placed Woods. Twelve-step programs, often the foundation of substance abuse treatment, are a staple of such facilities.

But they may not reach far enough, Kafka said. Many patients with hypersexual behavior relapse after 12-step programs, he said, because they haven’t addressed other issues in their lives. He believes that certain moods or psychiatric conditions cause sexual behavior to become disinhibited and abnormal.

This insight is not shared by the medical professionals I have had to deal with, who insist that relapse is the inevitable result of simply not being on the medications.

The article in its entirety can be found here.

Where are the mothers?

Are there any mothers out there who are willing to share their pre-natal experiences with a child who later received a diagnosis of schizophrenia?

When I started blogging about my son’s schizophrenia, I thought there might be other blogging mothers out there who were doing the same, but this doesn’t appear to be the case. There are many mothers who blog about their child’s autism, but where are the mothers who blog about schizophrenia? I am willing to widen my survey to include mothers of bipolar children (really, what’s the difference?). Mothers of bipolar children also are in short supply in the blogosphere.

Mothers need to be here and to be heard in order to do the job that mainstream psychiatry is unwilling to do. That job is to dig back into our emotional memory bank, into the pre-natal environment, to begin to piece together our child/ourselves story.

I thought that my ten month silent pregnancy was hugely significant in Chris’s later diagnosis, but the doctors were not at all interested. Not at all. So, I had to do the work myself, to piece together Chris’s unique life in utero and why I believe that the life before birth is very important, not in a pathological sense, but in finding a reason for someone retreating from life into a fantasy world.

We all know that there was something unique about the experience, and I suggest that if we think about it, we can pinpoint some unusual things about the experience from conception through birth. The reason I am interested in hypnotherapy, for example, is exactly because it can delve into the hidden world of the womb and even past lives. Try suggesting adjunct treatment in hypnotherapy to your mainstream psychiatrist and see where that gets you. They don’t want to go there. Most aren’t trained to go there. You appreciate perhaps more than they do the importance of the pre-verbal life.

So, where are you or your friends who have a story to tell about what was unsual/strange/remarkable about the pre-natal experience?

Medication – the low hanging fruit

There was a strange book review in the New York Times last week by Abigail Zuger. She managed to heap praise while smugly writing with a “didn’t I tell you so” attitude on Judith Warner’s new book, We’ve Got Issues: Children and Parents in the Age of Medication.

Strange because the reviewer took such obvious delight in Ms Warner’s sadder but wiser girl perspective about how she naively thought that the overmedication of children was a fact, and gosh, six years later she couldn’t find a parent out there who was thrilled about medicating her with drugs. This is news?

Dr. Zuger, an assistant medical professor at Columbia University, is entitled to her opinions, but she is unfortunately trying to present her opinions as medical truth. They are just opinions but will be construed as fact because she’s a doctor. Treating troubled children is more than symptom management for a calmer classroom: the medications seem actually to change the structure of the brain, helping it develop in what all evidence indicates is the right direction. More children in treatment should spell the beginnings of a healthier adult world.

What? Dr. Zuger is equating treatment with drug taking, not with treating the underlying problem. The “changes the brain for the better” argument is dangerous thinking and has no scientific basis but it sure is promoted by pharmaceutical companies. They, together with medical professionals pushing the enhanced brain function, have turned college students on to the perceived benefits of self-medicating prescription drugs for the purposes of competitive advantage. (Mother’s tip: Dr. Abram Hoffer’s niacinimide remedy for schizophrenia gives you focus with side benefits, not side effects.)

More children in treatment will lead to even more children in unnecessary treatment as our college students have demonstrated. There is a “me, too” effect here, and who can blame them? Similarly, if I were a mother of a school age child and observed that all the other kids had this competitive advantage, I would be tempted to ask why should my child be denied this harmless drug that protects the brain and increases focus? That’s discrimination, isn’t it?

Dr. Zuger goes out of her way to paint a disparaging picture of naive but caring twits like me who think that young children’s mental health should be managed in a different way. After all, almost nothing is known about the effects of antipsychotic medications on developing brains, reason enough to stay away from them. The effects on developed adult brains are pretty awful, the effectiveness of the medications are being widely questioned by science, and then there is the obesity problem. Why would we foist the same problems on children?

The answer to why we do this despite knowing the risks is found in the same article. There are only 7000 child psychiatrists in the United States. Lack of insurance and/or geographical access to psychiatrist means that most children will never see a psychiatrist, or else that one psychiatrist you do have access to is going be extremely overworked. Time, money and access being a problem, it’s cheaper for psychiatry to go for the low hanging fruit. Medication is that low-hanging fruit.

I see it this way. Your child (or the child in you if you are an adult) is being sacrificed for the “easy” solution, which is always the cheap solution when society is looking for mass “fix-its.” Mental health, unfortunately, does not lend itself well to one size fits all solutions. Increasing the number of child psychiatrists is a good idea if children and families are helped to find non-drug ways of dealing with their problems. (The job I naively thought psychiatrists were suppposed to be doing in the first place.) If it leads to a proportional increase in the number of children on psychiatric drugs, the potential benefit has been lost.

So, let’s call medication what it is, which is a cheap intervention, but let’s not pretend that it is something more noble than it is or that medication will somehow “protect the brain” when there are other therapies and ideas out there that work and which don’t produce side-effects. The poorer you are, the better your chances that you’ll be handed a drug and told to go away.

Musings from a mother

Dr. Amy Bishop, accused of killing three professors at the University of Alabama and wounding two others, was never charged when she accidentally killed her 17 year old brother in 1986. It appears that her act was just swept under the carpet, no doubt by her family. The question I would like to see answered is whether her parents insisted on psychiatric intervention for her at the time. I suspect not, because Dr. Bishop went on to rack up a number of years of further academic study in a relatively short time. Getting her head in order would have come at the expense of academic achievement. Therapy would also have revealed a possible motivation in her brother’s death, therefore ruling out therapy as an option for parents anxious to put it behind them.

Redeeming herself by being academically and profesionallly successful at her brother’s expense, as her unpublished but seemingly autobiographical novel is reputed to imply, is misguided altruism in the extreme.

Home Sweet Home

Reading Ron Unger’s post on the successes of the Family Care Foundation in Sweden has reinforced to me the value of staying the course with Chris, not getting stressed/worried/demanding, he will continue to be fine. The Family Care Foundation uses surrogate families and little meds. The families attend training sessions and receive group therapy and individual therapy and professional supervision. It sounds terrific, but begs the question as to why a surrogate family and not the genetically related family?

While it is generally acknowledged that a supportive family is a good predictor of recovery, it is also true that close family members, particularly the parents, are also the people most negatively impacted, i.e. feel that they have the “most to lose” if things don’t go well. This makes them in some ways not the best people to smoothly handle their child’s crisis. Looking at this another way, am I going to lose any sleep if my neighbor’s relative is not making his milestones, sleeping in and depressed or psychotic? Probably not. But I do care if it is my child and this concern will spill over, and in trying to be helpful, I may be creating further stress.

Another question that popped into my head on reading about the Family Care Foundation in Sweden, is how come it always seems to work in Sweden? I could use some therapy myself but I am not too keen on having strangers supervise me, having had to deal with psychiatrists for far too long who have turned Chris’s breakdown of spirit into prolongued medical meddling. North Americans have this view of Europe as much more sensible and humane when it comes to these matters, but is the reality really as good as they say it is? I live in a country with an illustrious past in psychiatry. The program that my son spent two years in was, in my humble opinion, no different than what you get in North America or other industrialized nations. It was all about the meds. The program was touted as being innovative (it has social workers and occupational therapists), but the reality was far from it.

Apart from the fact you are turning a personal family crisis over to management by others, the Family Care Foundation looks like a model worth emulating. Again, why just Sweden?

Watch this one take off

Thanks to Gianna Kali for alerting me to this article (article no longer available) in the Psychiatric Times: Opening Pandora’s Box: The 19 Worst Suggestions For DSM5. Dr. Allen Frances was the chair of the DSM-IV Task Force and is professor emeritus at Duke University School, Durham, NC. An excerpt from Dr. Frances’s article appears below.

The road to hell is paved with good intentions. Since when is a risk a syndrome? When the DSM says so, apparently. Watch Psychosis Risk Syndrome take off. What could be more humane, after all, than preventing young people (and their families) from (in theory) the avoidable pain of mental illness? The reason I am raising my own alarm here is that early intervention programs appear to pay no heed to mental illness as a deep-rooted coping mechanism that is a response to a trauma in the particular individual’s family background. Mental illness comes from somewhere, and you need look no further than than your own family to begin to understand that the problem is psycho-spiritual not biochemical in origin.

Sure, early intervention programs have staffs of psychiatrists, social workers, psychologists, etc. Their presence lulls people into believing that the psychospiritual and personal origin of mental illness is being paid attention to, and it is not. Resolving schizophrenia, for example, often takes some very intense therapies that don’t exist in these programs. If there is any early intervention program where Transactional Analysis, Family Constellation Therapy, Direct Confrontation Therapy, etc. are the mainstays, please let me know. Let me know, too, if there is a program that incorporates energy medicine into its daily routine. People are duped into believing that the mere presence of staff psychiatrists and other professionals is sufficient focus on the problems of the individual, whereas in reality they are there to deal with the effects of the medication while treating all individuals alike.

Dr. Frances writes
The Psychosis Risk Syndrome is certainly the most worrisome of all the suggestions made for DSM5. The false positive rate would be alarming―70% to 75% in the most careful studies and likely to be much higher once the diagnosis is official, in general use, and becomes a target for drug companies. Hundreds of thousands of teenagers and young adults (especially, it turns out, those on Medicaid) would receive the unnecessary prescription of atypical antipsychotic drugs. There is no proof that the atypical antipsychotics prevent psychotic episodes, but they do most certainly cause large and rapid weight gains (see the recent FDA warning) and are associated with reduced life expectancy―to say nothing about their high cost, other side effects, and stigma.

This suggestion could lead to a public health catastrophe and no field trial could possibly justify its inclusion as an official diagnosis. The attempt at early identification and treatment of at risk individuals is well meaning, but dangerously premature. We must wait until there is a specific diagnostic test and a safe treatment.

Captives in our own land

I am breaking my own rules about lengthy posts because I want to highlight in bold all the areas in Marvin Ross’s Sept. 2009 presentation to the Ontario Legislature where I feel strongly that he perpetuates the very reasons why people are not recovering from schizophrenia fast enough and in large enough numbers. While it is obvious that he is well-intentioned, his view of schizophrenia contributes to society’s high Expressed Emotion surrounding schizophrenia. Fear is a terrible incentive when struggling to get well. It cripples you before you can even begin. Fear has a handmaiden named guilt.

I feel that my son lost a minimum of two good years because I paid attention to the fear-mongering that I highlight below. Fear is not a good basis for making public health policy. Mr. Ross has bought hook, line and sinker what the pharmaceutical companies are peddling. He is obviously a fan of Dr. E. Fuller Torrey, who introduced me to the term “anosognosia,” a laughable term were it not taken so seriously by so many, meaning an “inability to accept the fact that you are sick.” How sad!

Of course there are too many people who need help and are refusing it or not able to access it. However, forced treatment by ineffective yet powerful drugs is no treatment at all and is a human rights abuse. There are effective treatments and strategies out there, some of which I highlight in my blog, but they are individualistic. Public health policy goes for the low hanging apples and a one size fits all approach. We have seen how successful governments are with this approach (not very).

I’m a parent, too, who couldn’t agree less with Mr. Ross’s solutions. In fact, many of the areas highlighted below I found to be simply untrue in my son’s case. My son is not a unique case, by the way. But I clung to the fear that if he didn’t take drugs he would relapse, if he relapsed he would be less and less able to recover, and the more I clung to these ideas, the less likely it was that he would recover. Fear is a not a good motivator. If you want your relative to get well, please have the courage to take issue with the status quo. This is all about your relative getting well. People should pay more attention to how well their relative is faring, and stop trying to worry about and think for others. If you want a solution imposed by society on your relative, lobby for the cheap, one-size-fits-all ones.

The presentation in its entirety can be found here.

Excerpt:

My friend, Ian Chovil, who I have written about is a case in point. He spent over ten years living on the streets with undiagnosed schizophrenia, addicted to drugs and alcohol.

In 1985, he was living in his car in Toronto when he was arrested. The courts sentenced him to 3 years probation and required him to see a psychiatrist. This he did in Guelph. He improved sufficiently that he was able to eventually get a job at the Homewood, a world famous psychiatric facility in Guelph and set up and maintain a very good informative website on schizophrenia. He is now retired. His website is chovil.com

He commented to me that “it is only too self evident to me that I have permanent damage that I must live with because I was not treated in the first six months. It is something that I think about everyday, something that I have to re-accept every morning.”

The longer that schizophrenia goes untreated, the more brain damage there is. The more frequently one has severe relapses, the longer it takes to recover and that recovery is not back to the same state the person was in before the relapse.

One of the reasons for this state of affairs is that many in society still do not recognize psychiatric illnesses as real diseases. Look at the recent report from the Ontario Ministry of Health called “Every Door is the Right Door”. A commendable attempt to improve conditions but they talk about prevention.

If they truly recognized psychiatric illnesses as diseases, they would not talk about prevention. After all, how can you prevent something when you don’t know what causes it. We can prevent a lot of heart disease, skin cancer and type II diabetes through life style changes because research has uncovered some of the factors causing those diseases.

Medicine cannot prevent diseases like Alzheimer’s, MS or ALS because it does not know the cause. Similarly, medicine cannot prevent schizophrenia or bipolar or depression because no one knows what causes them. We have theories and ideas but as of now, we do not have any understanding that could lead to primary prevention. And secondary prevention is just what I talked about a few minutes ago: early diagnosis, early and adequate treatment, rehabilitation, and health maintenance.

Schizophrenia is a disease of the brain that just happens. It is not a “mental health issue” a term that is often used. We don’t talk about people with insulin dependent diabetes as people with pancreas issues. They have a disease. Schizophrenia is a disease that causes or is caused by significant changes in the brain. There are well documented structural abnormalities, neurological abnormalities, neuropsychological abnormalities, electrophysiological abnormalities, and cerebral metabolic abnormalities.

And these changes have even been documented in people who have never been treated although the opponents of drug treatment would argue that the changes are the result of prescribed medicines and nothing else.

Imaging studies of the brains of untreated people with schizophrenia have shown that there are significant differences when compared to the brains of matched healthy people. The effect of antipsychotic drug treatment on these sick patients results in their brains gradually starting to resemble the brains of the normal healthy controls.

The people you see pushing a shopping cart with all their worldly possessions in it while mumbling incoherently to themselves, or shouting rhetoric on the street corner, or living in a cardboard carton are sick. They deserve humane care, humane consideration, and treatment.

SO WHY AREN’T THEY?

A large part of the reason is that we allow them to make their own treatment decisions – something they do not have the capacity to do. Part of their illness is their inability to understand. This is a condition called anosognosia. They are so sick and delusional that they do not know they are sick and refuse treatment.

And our society thinks that is OK. Most opponents of compulsory treatment cite John Stuart Mill’s On Liberty. Mill said that “the only purpose for which power can be rightfully exercised over any member of a civilized community, against his will, is to prevent harm to others.”

When Mill wrote that, there were very few medical treatments for anything, let alone psychiatric disorders.

But, Dr. Richard O’Reilly, a psychiatrist in London, Ont and the former president of the Ontario Psychiatric Association points out that Mill also said in the very next paragraph, “those who are still in a state to require being taken care of by others must be protected against their own actions as well as against personal injury”

We do that for the elderly with serious dementia and Alzheimer’s. We do not allow granny to refuse treatment for her dementia and to live in a refrigerator box outside so why do we do that for young people with schizophrenia? It is cruel and inhumane for any caring society such as ours to allow people who are sick to remain sick.

In fact, the most effective anti stigma strategy is not to try to educate the public but to provide treatment for those who need it. Tragedies like the Virginia Tech shooting or the Greyhound Bus beheading only fuel negative views about mental illness. Preventing these events by providing treatment for those who commit them or who are likely to commit them do much better.

Psychiatrist Dr. Sally Satel, said in the New York Times that “no matter how sympathetic the public may be, attitudes about people with mental illness will inevitably rest upon how much or how little their symptoms set them apart.”

In the western world, with growing affluence, increasing attention to civil liberties, in the 1970’s mental health laws changed. They were re-written to protect individual rights. I am told that the authors of Ontario’s mental health act did not expect the result that has become so obvious over the past twenty years.

They thought the mentally ill would still get good treatment but within that right to receive treatment, their other rights would be protected. At the time cynical psychiatrists often joked about the mentally ill now being allowed to die in back alleys with their rights intact. The laws created due process, caused a careful examination of forced treatment, but were ultimately based on a fantasy that those without insight into their illness could make sound treatment decisions..

And the result has been that many seriously mentally ill have lost their right to treatment.

In several European countries, the same countries that have excellent social welfare systems, excellent systems for the care of the mentally handicapped, and countries that are renowned for their approach to civil liberties, it has been recognized that we threw away the right to treatment when our laws over-emphasized the civil rights of the mentally ill. And in these countries the laws have been modified to correct this. And it is the attitudes, resources, rules, practices and laws of these countries that we should study and emulate.

In conclusion, I would like to pass on some comments from my family. My wife suggests that if our health system cannot do a better job of providing treatment for people with schizophrenia, then we (the families) should all be given free antidepressants.

My son works for a psychiatric rehabilitation program in Hamilton as a peer counsellor. Both he and the agency are in Ms Horvath’s constituency. The government has just cut off their funding. As a result, the clients will lose their support and the peer support workers, for whom this job helps with their self esteem and feelings of self worth, will be unemployed.

Thank you for your time today and, as promised, I will leave you with a copy of my book. Please don’t feel any pressure as there will be no test if you do read it. I am also leaving you with the DVD of the feature film Cutting For Stone which is going into general release in the US in October. The film was shot in Hamilton, Ontario, written by a psychiatrist and is one of the most realistic depictions of schizophrenia that you will find. The bonus scenes added to the DVD are very educational.

Something is changing

Chris rang me today from his mobile to say he had, on the spur of the moment, gone to a Giacometti exhibition. He sounded very much alive. There is something exciting going on with Chris that has been building slowly for months. It is in the way he engages with others, even in the way he watches television. His voice has suddenly taken on an enthusiasm and conveys a purpose. He occasionally expresses boredom, which is a hopeful sign.

Last night I was struck by the fact that he stayed up to watch a television show, alone. While this sounds mundane, for an observant mother it is anything but. He has approached pleasure in the past with a sense of duty or out of respect for someone else. Last night he was doing what he wanted to do, on his own terms.

This building up of the personality is a long, arduous process. There are times, like with a mental breakdown, when the personality, however fragile it was, seems to completely disappear under layers of apathy.