Saturday, May 31, 2014

And now for something warm and fuzzy!




Psychiatry these days --- I could do link after link and commentary after commentary about guns and violence and mass shootings and can we prevent all this?  But why?  Let's go for something sweet and warm and fuzzy and ducky today.  I hope you enjoy the video above.

Tuesday, May 27, 2014

Just a Phase?



Today's Shrink Rap post is located over on Clinical Psychiatry News.  "Distinguishing the killers among us" is a story I've written about before here on Shrink Rap, about a situation I dealt with in high school. 

 The timing seemed right to tell the story again. 

Thursday, May 22, 2014

Maryland work group on legislation regarding involuntary care needs PATIENT input!


On May 20th, I attended the Maryland Department of Health and Mental Hygiene (DHMH)'s first Outpatient Services Programs Workgroup, designated by Senate Bill 882/ House Bill 1267.  These were bills proposing legislation to bring outpatient commitment ("assisted" outpatient treatment - AOT) to Maryland and to look at the use of ACT (assertive community treatment) and other outpatient services in Maryland.  The meeting was the first of 8, and they are open to the public.

Since involuntary outpatient treatment is a controversial topic, it's no surprise that the room was full and all the stakeholders were represented.  I'm going to guess there were 120 people there, and I saw people from NAMI, TAC, the public defender's office, the psychiatric society and our diligent lobbyist.  One thing that surprised me was when one man announced that he was one of only three consumers there.  Really?  This is about legislation that might impact people with psychiatric disorders, shouldn't they come to have a say?  I spoke with this gentleman after and was told there was no transportation available to bring people them from their day programs.  But really, aren't there people out there who have been committed to hospitals, who might be concerned about this legislation, who have cars? I guess they'd need to get time off work, as I did.  I also think it's possible they didn't know about the meetings, so I'm posting this here.  I knew about it because I'm on the psychiatric society's legislative committee, and obviously another hundred or so other people knew about it, but if you know someone who might like to attend, please spread the word.  Please be aware that the meetings may be moved to a larger space. 

I hate the idea that stakeholders make these decisions for people -- some of whom are quite outspoken and organized -- without their input.  Those who've benefited from forced care need a voice. And those who've been harmed by forced care also need a voice.  If you have something to say, or you just want to listen to the process, these meetings are open to the public. 

Per Facebook:
DHMH to Convene Behavioral Health Integration Stakeholder Workgroup: Members of the public invited to participate

The workgroup will make recommendations on issues related to behavioral health, including statutory and regulatory changes to... See More

Monday, May 19, 2014

Can Medication Prevent Crime?



Ah, not here, not now, but over on Clinical Psychiatry News, ClinkShrink looks at the question of whether medications can prevent crime and she talks about a study in Sweden that was recently published in Lancet.  Let me redirect you over there:
 Can Medication Reduce Crime?

Sunday, May 18, 2014

The HIgh Cost of Forced Outpatient Care


I'm going to refer you to a long article in The Herald News,  Focus: Safety concerns prompt states to revisit involuntary commitment laws that address the mentally ill.  

Now I'd like to bring you to the end of the article where there is mention of the fact that President Obama has authorized $60 million to fund these programs.  If we divide that evenly between the states, it's about $1.2 million per state.  New York already has a program for involuntary outpatient commitment called Kendra's law.  The studies have shown that it has been successful in decreasing hospitalizations and incarceration.  The costs are calculated  per person "before" and "after" involuntary commitment, so the amount of money shelled out for each patient goes down when they've been put in the program.  What isn't reflected in the cost, is the overhead and infrastructure that New York State put in place to increase services.  I will point out to you that Kendra's law is mostly used in New York City, around Albany, and a few other hot spots, but not in the rest of the state.  And how much money has this successful program cost to implement in these populated parts of New York?  From the website of the NY Office of Mental Health:

Kendra's Law: Final Report on the Status of Assisted Outpatient Treatment
Resources to Provide Court-Ordered Services

The Governor's budget for Fiscal Year 2005-2006 provides more than $32 million for operation of services in support of Kendra's Law. This appropriation continues State support of case management and other services aimed at keeping recipients in a treatment program, including psychiatric medication as required. Since Kendra's Law went into effect, Governor Pataki has also acted to expand access to case management and other key community-based mental health services that would be needed by individuals receiving court-ordered treatment, as well as many other individuals with severe mental illness who have less intensive, but still substantial, service needs. The Governor's budget for Fiscal Year 2005-2006 also provides more than $125 million in ongoing funding for such services. This "Enhanced Community Services" funding has been used to both improve and expand the capacity of the existing community-based mental health system and to strengthen the cohesiveness and coordination of that system. More specifically, Enhanced Community Services were designed to steer the New York State mental health system toward a more person-centered, recovery-oriented service delivery approach, and were targeted for the following purposes:
  • to expand case management, Assertive Community Treatment (ACT), and housing services to support community integration;
  • to develop Single Points of Access (SPOA) to better manage service access and utilization; and
  • to increase the availability of other services that enhance community participation and improve the engagement, quality of life, and satisfaction level of service recipients.
---------------
 Many states have involuntary commitment laws. Few of them implement them, as the Herald News article highlights.  It costs too much.  $60 million is not going to do it for a country of 300 million people.  And while we do know that the program reduces hospitalizations and incarcerations in this vulnerable group of very ill, high users of emergency mental health services, what we also know is that the recipients don't like it; satisfaction rates are low (---that statistic doesn't make the news, presumably because no one cares?)

Finally, the article ends by pointing out that involuntary outpatient commitment is not about forcing medications.  This is a common saying of those who support it, but when legislation was proposed in Maryland, the legislation included an order for a specific class of medications and procedures to make changes or contest it.  If a judge tells you that you have to take a medication or you can be brought by the police to a hospital for evaluation, how is this not forced medication? 

Friday, May 09, 2014

Tell Me About Sweden

I've been delving into a recently published study from Sweden that was mentioned here in the Wall Street Journal. The study looked at the effects of psychiatric medication compliance on violent crime. It's interesting and intriguing but I have to say I'm struggling to see how or if this may be applicable to people in the United States. Thus, this blog post. I know from Google analytics that we've had almost 5000 page views from readers in Sweden this month alone. I know that many of our blog readers are patients. Please, tell me about your mental health care system. From the paper I know that your legal system is very different from ours: you essentially have no insanity defense. It appears that the only time mental state issues come into consideration is at sentencing. This means we really can't know how many of those violent crimes actually were due to psychiatric symptoms.

But beyond that fact, I'd like to know how the community response to mental health issues may be different and about differences in the system of care.

Some questions, off the top of my head:
-Are there mobile treatment teams that respond on site to patients in crisis?
-What is the emergency evaluation process, how long does it take, does it work?
-If there is an emergency response, how often do patients get taken to a hospital vs some other alternative?
-What are the involuntary medication laws like? How often is this pursued? How often ordered vs not?
-Are outpatient services integrated with substance abuse treatment and medical care?
-How long does it take to get into outpatient treatment?
-Is there legal enforcement for outpatient treatment? What does it look like? How often is it sought?
-Are there pretrial diversion programs for mentally ill people who get arrested and charged with crimes?
-Any thing else you'd like to tell me?

Don't be limited by my questions. I have trouble believing that a single intervention like medication should have such a significant impact on crime. Disclaimer: this is probably going to be my next Clinical Psychiatry News column, so you may be quoted.

Wednesday, May 07, 2014

Privacy versus Necessary Communications



Greetings from New York.  All the Shrink Rappers have been enjoying the APA meetings these past few days.  

Today's post is located over on the Clinical Psychiatry News website: Legislation's privacy exceptions of psychiatric patients are concerning.  Do surf over and read the post there. 

Wednesday, April 23, 2014

No Easy Answers



Today's post is brought to you by Steve Lopez of the LA Times and is located over on Pete Earley's blog.  You can click HERE to read the touching story of Nathanial Ayers, a talented musician who suffers from schizophrenia and does not want to take medication for his condition.  On his third court appearance, a judge appointed a relative as conservator for Mr. Ayers so that medications can be given.  It sounds, from the article, like Mr. Ayers had intolerable side effects to an older anti-psychotic medication and has never been willing to try the newer, atypical anti-psychotics which have more favorable side effect profiles --unless, of course, you're the person having the side effects, in which case the "profile" may not matter.  Please read the article over on Mr. Earley's blog, then come back here to read about my thoughts.

So I'm hoping that the story has a good outcome, and here are a number of things that may happen here.  I go from best possible outcome to worse possible outcome, and feel free to shuffle the order on the shades of gray:

  • Best:  Mr. Ayers takes the medication, it works, his symptoms resolve, he feels better emotionally, and he is able to function better, and he has no side effects and decides he wants to continue it.  This would be the happy ending we all want to hear.
  • Mr. Ayers takes the medication with resolution of his symptoms, improved functioning, and no side effects, and no appearance of metabolic syndrome, but he does not recognize that he is doing better without the medications and wants to go off but the court insists he continue.
  • Not bad: Mr. Ayers takes the medication and it works with resolution of his symptoms and improved functioning, but he has side effects.  He decides the improvement is worth the side effects and chooses to continue taking the medication.
  • Mr. Ayers takes the medications and it works, but he has intolerable side effects and needs to go off it.
  • Mr. Ayers takes the medication and it works, but he has  side effects and the courts make him continue with a medication that makes him feel bad 
  • Mr. Ayers takes the medications and it doesn't work, so he stops taking it.
  • Mr. Ayers takes the medications and it doesn't work, but the court insists he continue taking it.
  • Mr. Ayers takes the medications and it doesn't work, and he has  side effects, and the court insists he continue taking it.
  • Mr. Ayers takes the medications and it doesn't work, and he has intolerable side effects, and the court insists he continue taking them and then has a stoke or heart attack or diabetes which may have been brought on by the metabolic effects of the ineffective, intolerable medication that the court made him take.  
  • The medication works and the patient stops it and has a tragic outcome, either for himself or for others.  
Unfortunately, what makes the scenario even harder, is that the medication may partially work or be  somewhat effective -- so perhaps a given patient is less irritable or combative, which makes it easier to manage him or her -- but still hears distressing voices or experiences intolerable emotions.  We don't know exactly how long to wait, how high a dose to give, or how many medications, alone or in combination, we need to try before we're sure there  is no adequate treatment.  Also, the tolerability of side effects and the acceptibility of risk are things that may be difficult for one person to make for another.  

This is a long way of saying that unless the patient has a positive response that he appreciates, the issue is not a simple one; it can be complex and nuanced in a way that many of the parties may not appreciate.  If our medications worked more reliably, and did not have side effects and pose the risks (risk, not certainty) of decreasing both the quality and quantity of life, then forced medication would not be such a difficult option.  But the issues of limited efficacy and tolerability exist before you even begin to address the civil rights of a person to decide their own care.

I hope we'll hear about the outcome from Mr. Lopez, and I do hope Mr. Ayers has a good response and decides, on his own, that he'd like to continue the medication.  And if it doesn't work, I certainly hope the court does not force him to take an ineffective agent that he does not want.  In our "meds are good" society, it's not that unusual for people to be on medications long after we've lost track of what it was we trying to target with them.
 ------------------

On a different note, I spent my day with a police officer today who does crisis intervention.  As we stated the day, he received an email from a patient he had petitioned to the hospital 2 years ago, thanking him for forcing her to get care and for saving her life.  It was my feel-good story for the day.


Sunday, April 20, 2014

Interesting reading around the web



Happy Easter!  ClinkShrink has become obsessed with photographing birds, and I've suggested that for today, she give us a rabbit or two.

First, I'll send you to Clinical Psychiatry News where Clink discusses the latest report from the Treatment Advocacy Center on how there are 10 times more people with mental illness in jails than in psychiatric hospitals.  See Report suggests reform for mentally ill in prison.

Next, I'll send you to the New York Times for a very thoughtful article on the use of antidepressants.  See Doris Irovici's article on The Antidepressant Generation.

Then I'm going to send you to Pete Earley's blog where he talks about the split in support on the Murphy Bill in Congress, HR 3717 which both increases resources for community mental health centers and increases reliance on involuntary treatments. 

Finally, I'm going to lead you to a post from one of my Twitter followers, "Sectioned @ mental health" who writes a touching post on things learned about the civil commitment process in the UK, the hard way.  See Unexpected Knowledge-- things I've learned since being sectioned. 

Thanks for reading!

Tuesday, April 15, 2014

Does bad parenting cause mental illness?


Over on our Facebook page, a reader posted: 

Supporters of families should protest SAMHSA's distribution of its new "Family Therapy Can Help" booklet. It's full of statements that imply that faulty family dynamics are the underlying problem in the development and persistence of mental illnesses. At the same time, SAMHSA does nothing to educate the public or clinicians or people with severe illnesses on what is known about psychotic disorders from a science based perspective. Here's a link to this free document:
http://store.samhsa.gov/shin/content//SMA13-4784/SMA13-4784.pdf

Around the same time, a Shrink Rap reader wrote in to us saying:

    I get tired of the stories about the noble families caring for their wayward child. It's that way sometimes, but a lot of times, it's NOT that way!
   What I don't understand is this: I have NEVER EVER read an article anywhere that talked about families and an adult child with serious mental illness that did anything but praise the family of origin and their noble quests to save their unfortunate children. (Well, on Dr. Allen's site, which is like the only exception).
   I have bipolar and came from an incest family. Just about every psychiatrist I have ever seen, and every single community mental health worker (social services) has said that so many of their patients come from abusive families. In fact, the community workers who only see people with serious and persistent mental illness say that nearly ALL their clients have extremely abusive families.
   So what is going on here that there is NEVER EVER a mention that perhaps some of these sacrificing, noble family members may have been the catalyst for the mental illness and are continuing to abuse the person by committing them and placing all the blame of the messed up family at the feet of the one who has a label? And bipolar or schizophrenia labels are handy for parents or other abusers to escape culpability.
   I understand that NAMI is all about moms not wanting to be blamed for their kids' mental illnesses, which probably did happen unfairly quite a bit. But come on! Often parents are the major cause, by abusing or failing to protect their kids (in my sexual abuse support group, all the ladies were blamed and ostracized by their moms and others when they told about what happened. What I learned from that is that kids who are abused and their mom has their back don't end up so messed up that they need to be in a support group)
   So it always ticks me off when I read blogs written by mental health providers, or newspaper articles, or see something on TV showing these wonderful, loving parents, and come on, statistically, some of those families are probably very abusive and the motives for promoting involuntary commitment are very dark indeed, a legal way to continue abusing an adult who has tried to escape.
  And keep in mind that many people who have been in a mental hospital found it to be further abuse.
  Or did all those mental health workers lie to me about mental patients and their toxic families?
 
Clinically, I've seen all combinations.  I've seen people with really dysfunctional families and very sad histories that have included horrible losses and abuse, who have turned into very functional, loving, and productive adults.  I've seen people who have been raised by wonderful parents have serious mental illnesses, and I've seen people with awful family lives who have been come seriously mentally ill.  It's often hard to sort out the role of genes versus environment, because often the dysfunctional and abusive parents also suffered from mental illness.   People differ with their individual sensitivities to what has been sad and done to them -- some feel injured by parents who seem to have good intentions but sometimes say the wrong things, and others have no problem dismissing what sounds to be flagrant abuse.  Certainly, objectively traumatic events color who people become and how they react to the world.  But does childhood trauma cause psychotic disorders?

What do our readers think? 

Saturday, April 12, 2014

Medicare Payments to Docs Gone Public


Today's post is over on Clinical Psychiatry News where I wrote about 
"Privacy or Transparency: Maryland psychiatrists speculate on Medicare payments and their accessibility to the public."

Please surf over there to read, then return here if you'd like to comment.  The CPN site is not taking comments lately. 

Sunday, April 06, 2014

Dear Congressman Murphy: Regarding HR 3717




American Enterprise Institute, AEI, a conservative think tank, held a panel on Fixing The Mental Health System, What Congress Can Do.  I posted the discussion above, the talking begins at 12 minutes.  The panel is introduced by Dr. Sally Satel, and the speakers include:

  • Congressman/Psychologist Tim Murphy who talks about legislation in Congress, HR 3717.  This bill pushes the federal government to provide more services -- a good thing -- and it also ties in requirements for Involuntary Outpatient Treatment (also known as Assisted Outpatient Treatment or AOT).  The New York Times has discussed this in Mental Health Groups Split on Bill To Overhaul Care.  
  • Dr. Jeffrey Lieberman, the President of the American Psychiatric Society
  • Dr. E. Fuller Torrey of the Treatment Advocacy Center
  • Former Congressman Patrick J. Kennedy
If you'd like to watch the event, the video is above, if you want to read about it, read Here. 

I don't want to dwell on the issue of involuntary treatments today, but instead, I'd like to make some comments on H.R. 3717 The Helping Families in Mental Health Crisis Act.  I've read about the bill, I have not read the full text, but if you'd like to, it's here. 

Dear Congressman Murphy,

I'm no fan of HIPAA, as a physician, I find it makes it more difficult to get information from other clinicians.  Your point, however, that HIPAA prevents a doctor from getting information from a family is not quite right and you were more on target when you said it was misunderstood.  Physicians can listen, and families can talk, but privacy laws mean that physicians can't release information without the patient's permission.  Actually HIPAA defines all sorts of entities that can get medical information, but there is nothing in it that says a family member can't tell a physician about their concerns or relay past history.  Sometimes, clinicians refuse to release information to families or even other physicians, citing HIPAA, when in fact, they haven't specifically asked the patient for permission.  Sometimes doctors or facilities are lazy, sometimes they are misinformed, and sometimes they are afraid of being sanctioned or sued so they err on the side of being overly careful about whom they communicate with.  For the most part, I don't believe that doctors should release psychiatric information unless a patient consents to this.  Lets hope that everyone's judgement on these issues gets a lot better. 

In talking about access to care and a shortage of psychiatrists, because psychiatrists are in such demand, many psychiatrists have chosen to opt out of participating with health insurance.  I've written about that Here.  Part of the access problem lies with the fact that insurance companies either restrict patients to seeing in-network psychiatrists, or reimburse less if patients go out of network.  At the same time, insurance companies will list psychiatrists as being in their network when they are not, creating the false impression that the network has plenty of providers: see this Wall Street Journal Article.   So what about increasing the number of available psychiatrists by requiring insurance companies to reimburse the same for both in-network and out-of-network treatment when access to care becomes difficult?  If a family is told that the next in-network appointment is 6 weeks away, but an out-of-network doctor can see them the next day, should the insurance company really be permitted to save money and reimburse less?  And should insurance companies be permitted to have "Usual and Customary" rates that are far below the community standard?  And perhaps if Medicaid and Medicare would reimburse for out-of-network services (they don't), the number of treatment options might open up. 

Finally, you talked a lot about the standard of "imminent danger" as being too high standard for hospitalization.  That's all well and good, and I agree with you that we shouldn't be waiting for metastatic disease (as your comparison mentioned) to begin care, on an inpatient unit if needed.  But it's not just about that standard of care for forcing treatment, it's about what insurance will reimburse for.  Have you ever tried to admit a patient to a hospital?  Insurance companies generally will not authorize treatment for psychosis alone.  The only level of illness that they will authorize inpatient care for is the same level that one needs for involuntary commitment: imminent dangerousness.  So you can drop the level of illness it takes to get a patient admitted -- and I presume you mean by allowing for involuntary treatment -- but does it matter if the law changes to a "need for treatment" standard if insurance companies don't agree that the patient needs treatment?  I asked a woman the other day why she didn't sign herself in voluntarily after a serious suicide attempt -- she was being transferred from an ICU and was distraught that she was being 5150'd (California lingo).  She told me the doctor said the insurance company wouldn't pay for the admission if she wasn't committed, otherwise she would have signed herself in.    One ER psychiatrist I know was asked by the insurance company if the patient's gun was loaded.  Does that matter?    If the Navy Yard shooter had been brought to the hospital by the police, as he should have been, they may well have let him go if it was believed that insurance wouldn't pay for an inpatient stay.  And while severely mentally ill people may have higher rates of violence, studies have shown that treatment deceases violence.  In fact, patients who are seen weekly after a hospitalization are half as likely to be violent as the general population -- voluntary treatment makes a big difference.  But getting that level of care for our patients in the public mental health system only happens with the few who get put with Assertive Community Treatment teams. 

One thing is clear, before we start forcing care, let's make sure there is even care to be had, and that those who want it, or can be encouraged to get it, have a means to do so. 


Friday, April 04, 2014

Book review: Viviane (a novel)

With thanks to Jed who thought I'd like this novel.

Take a deep breath before you get on this ride.  The twists and turns come fast, and the trip is short, but memorable, with moves that made me gasp.  So short, it's almost more of a novella, and that's good because a ride like this is compelling for hours; I'm not sure I'd want to be on long journey.  

Viviane is dark and mysterious, the psychologically-laden plot pulls the reader along quickly, and if that's what you're looking for, stop here before I move you to plot spoilers.  It's a first novel by Julia Deck, translated from the original French by Linda Coverdale.

Very quickly, we learn about Viviane.  She is 42 years old and she has a 12 week old daughter, a peaceful baby who seems to never want for very much.  Viviane is the public relations officer for a concrete company, and her husband Julien can no longer stand being married to her; he's having an affair and "it isn't even from love but from despair."  He wants to leave, he needs air, but instead, Viviane leaves and moves into her own apartment.  Then she goes to see her psychoanalyst and kills him.  We are now on page 8.

The circumstances that led up to the murder of the psychiatrist are described.  Viviane was struggling.  Something needs to be done, I can't take it anymore.  Doctor, you're not listening to me.  He is insensitive, he implies that her problems are her own fault.  You'll take these pills for a few months, you know, the antidepressants, plus the ones for when your nerves give way, they help stabilize the hysteria.  She stabs him and leaves, taking the knife with her.

Viviane then proceeds to stalk, meet, and talk with those suspected of murdering the psychiatrist: his pregnant lover, his widow (who lives with her own lover), a young patient with a history of violence.  She doesn't just stalk the patient, she sleeps with him.  We learn about how her husband's lover was the woman who took her job while she is on maternity leave, how jealousy strikes her, and how she can't let go of dead mother's apartment.  All the while, Viviane is searching, and the reader (or this reader, anyway) waits to understand what could have motivated her to commit murder.  She is not, it seems, delusional. But Viviane arranges to meet Julien, and she stands back and watches him, not letting him know she is there.  This is her end, her part from sanity, and she lands in a hospital, where she confesses to the murder.  She is moved to another facility, one for longer term care, and oddly, the baby goes with her.   Oh, but the end comes with a jarring twist, and all we thought we knew was not to be, the entire landscape shifts from under us. 

That is the thing with this novel, it is constantly shifting.  The language is dark and we feel a distance from Viviane who remains an unknowable person, even as we move closer to know more of her, then farther away to see she is truly a stranger.  As we move in and out,  the point of view constantly shifts: at one moment the story is being told in first person singular, and the next moment it shifts to third person, or even second person.  In French it must be more intriguing, because there is the second person pleural, or formal, tense, one that can't be bridged in the translation to English. (Reviewer's note: finally!  Those years of college French I sat through, that evaporated from my brain no sooner than I left the classroom, have finally served some purpose.)  This constant movement feels odd, quirky, and most unusual.  It parallels the ever-shifting sense of reality that the book creates, where we don't know whose story it is, what truth is to be had, or where it will all stop.  A truly unique ride. 

Monday, March 31, 2014

Thank You, Pete Earley



Lots of good stuff on Pete Earley's blog lately.  He has a blog post up today with a video of hours of Congressional testimony on the topic of "Where have all the patients gone, examining the psychiatric bed shortage. This will be taking up some of my free time over the next days as I plan to listen to it all. There's also a video of the talk Virginia Senator Creigh Deeds gave at the National Press Club about access to care and his tragedy with his son.

Pete was also kind enough to put up a post for me.  I'm interested in talking to families for my book, and I asked my colleagues who are active with NAMI if any of the NAMI families might be willing to chat with me.  Pete's post resulted in calls from all over the country.  I heard from several parents with children who have been terribly ill, in and out of hospitals and jails,  stories filled with heartache.  One woman spoke at length about her son who has been ill for decades, and then mentioned that she'd also committed her daughter for a post-partum psychosis.  She thought the daughter was still angry about it, but when she told the daughter she was going to talk to me about committing others, the daughter said, "I hope she's in favor of it," and this was the first she realized that the daughter was glad she'd been forced to get treatment.  The son is still struggling, the daughter is doing well, working and raising her children.  One woman called to tell me her distress about being committed, and as we talked for a while, I told her I didn't think she'd actually been committed as there had not been any court hearing.  By the time we hung up, she told me she felt better and maybe it was time to let go of some of her anger.  Another woman who was distressed about having been hospitalized was upset because she felt the doctors should have been more aggressive about looking for physical reasons for her psychosis, and they missed her exposure to toxic occupational chemicals.  One woman told me of her child's struggles with illness and treatment, and about how helpful Assisted Outpatient Treatment had been in keeping her well.  At some point the patient had come to realize how much better she felt without her delusions and hallucinations and now she gets treatment willingly.  Finally, a man called to tell me about his struggles with schizophrenia.  He was hospitalized once decades ago, has never missed a dose of medication, and has been able to enjoy a full life, but his brother, who also has schizophrenia has resisted treatment and has been in and out of the hospital (he guessed 40 times), jail, and has lived on the streets, and never able to work.

It's been helpful to me to hear these stories, they add to what I know from my own experiences, and to the stories that our readers have been writing in our comment sections for years.  I'll ask that if your story is different than those I described, that you respect  that someone else might have had a different experience than yours and that you not write in to criticize or question the story that someone else relayed.  I only spoke to these people for a little while, so I don't know every nuance of their care,  but what I do know is that some people found involuntary treatment to be helpful for themselves or their family members, and some did not.

 

Thursday, March 20, 2014

Can You Make Docs Be Nice?


Today's post, called Legislating Kindness, can be found on our Clinical Psychiatry News column.  
Please surf over there for the post.   

They no longer have commenting ... I don't know why that is...but please come back here if you want to say something.