Skip to main content

Is This Really the Best We Can Do?

This is the view outside my hotel deck this afternoon in Half Moon Bay, CA. It's really beautiful. But it's not the view I was expecting.

I was expecting a grittier view as I visited for a few hours with my son Tim somewhere in downtown San Francisco's Mission Street area.

I travel a lot for my job as President and CEO of Mental Health America. When those trips bring me to northern California, I always try to build in some extra time so I can visit with Tim. Today was no exception.

I got up at 3:15 am to catch a 5:30 am flight out of Washington that got me to San Francisco by 11. I have something for work at 6, so I expected to have several hours with Tim.

But visiting with Tim takes planning in advance. Tim has schizophrenia. He has lived in San Francisco for the last decade. He has often been homeless, or in jail, or in treatment. Even when he has housing, he doesn't stay in one place very long, and he doesn't have a phone.

So I make my plans through the agency that serves Tim, and schedule everything far enough in advance that they can let Tim know I'm coming.

To be honest, having to plan this way can be a real pain in the neck - and I hate to impose on his extraordinarily patient caseworker to go out of his way for us. I do it because I love Tim and need to see that he's doing okay, and also because I really enjoy his company.

But, like too many other times I've come to visit, I didn't get to see Tim today. This time it's because he's in jail, and the jail doesn't allow visitors on Thursday afternoons - even if they've traveled 3000 miles to get here.

Tim got to jail this time the same way he typically gets to jail. He had been in jail, was sent to a program as a condition of his release, broke a rule in the program, had to discharge himself from it, and was re-arrested because that violated the conditions of his release. This all happened a few days ago.

Of course Tim should be accountable when he breaks the law. Mental illnesses aren't free passes to any and all bad behavior. But I fail to see how repeatedly locking up people with serious mental illnesses in custodial care institutions (called jails) for weeks or months at a time for status offenses serves any meaningful purpose.

It costs a lot of money. They don't get appropriate treatment. And they don't get better.

The bottom line is this. In 2019, this is still how we most frequently "treat" serious mental illnesses.

I get a nice view. Tim gets a jail cell. People are isolated. Family ties are broken. And no one recovers. 

Is this really the best we can do?

Paul Gionfriddo is President and CEO of Mental Health America and can be reached at pgionfriddo@mentalhealthamerica.net.


Comments

  1. I hope you will join us in focusing MHSA funds (and for that matter, the mental health industry) on the seriously mentally ill, like Tim. And expanding Laura's Law

    ReplyDelete
    Replies
    1. I created the B4Stage4 campaign for Mental Health America so that we would treat all mental illnesses seriously, and not just in their late stages after crises occur. We have to treat mental illnesses the same as we treat other chronic diseases - with early detection, far earlier interventions, and at every stage in the disease process with integrated health services that offer hope for recovery, even when cures are elusive or impossible. It's too easy to forget that custodial care didn't work in state hospitals a generation ago, just as it doesn't work in jails today.

      Delete

Post a Comment

Popular posts from this blog

The Missing Mental Health Element in the Ferguson Story

By now, everyone has heard the news from Ferguson, Missouri.  An unarmed 18 year old named Michael Brown was shot and killed by a police officer.  Michael Brown was black. Some of the events surrounding the shooting are in dispute.  But what isn’t in dispute is that for the past two weeks, a community has been torn apart by race – a community that until recently was best known for its proximity to St. Louis and its designation as a Playful City, USA . Picture credit: Health Affairs Media reports since the August 9 th shooting have focused almost entirely on one angle – race relations.  We’ve heard about unrest in the city, the National Guard, police in riot gear, and danger in the streets.  We’ve heard about the District Attorney’s ties to law enforcement, and concerns that a too-white Grand Jury may be racially motivated not to indict the police officer involved in the deadly shooting. But the media have been strangely silent about a different angle – this comm

Veterans and Mental Illness

On a sultry June morning in our national’s capital last Friday, I visited the Vietnam Veterans Memorial .   Scores of people moved silently along the Wall, viewing the names of the men and women who died in that war.   Some stopped and took pictures.   One group of men about my age surrounded one name for a photo.   Two young women posed in front of another, perhaps a grandfather or great uncle they never got to meet. It is always an incredibly moving experience to visit the Wall.   It treats each of the people it memorializes with respect. There is no rank among those honored.   Officer or enlisted, rich or poor, each is given equal space and weight. It is a form of acknowledgement and respect for which many veterans still fight. Brave Vietnam veterans returned from Southeast Asia to educate our nation about the effects of war and violence. I didn’t know anything about Post Traumatic Stress Disorder when I entered the Connecticut Legislature in the late 1970s.   I had only vag

Celebrating Larissa Gionfriddo Podermanski Five Years Later

My daughter Larissa died of Metastatic Breast Cancer five years ago, in May of 2018.  She had only two wishes at the end. One was that we plant a tree for her. We did - in a Middletown CT city park - and it has grown straight and tall. The other was that she not be forgotten. Larissa's family and friends took pains to reassure that she could not be forgotten. If you were fortunate enough to know Larissa, you would know why. Still, I wondered how I might celebrate her a little more now that some years have passed, while sharing some of her memorable spirit with others (some who knew her and others who did not), while reminding us why she was such an extraordinary woman. In early 2017, Larissa started a blog called Metastatically Speaking, through which she chronicled her life with MBC. Unfortunately - and through no one's fault - her blog disappeared some time after her death. So, if you search for it now, you can't find it.  However, I was fortunate enough to see and retain