Category Archives: Stigma

Thank you Project UROK!

A few weeks ago I was on one of my favorite sites, Upworthy, when I came across a story called What’s it like living with mental illness? Ask Wil Wheaton. It included an amazing video in which actor Wil Wheaton talks about his experience with mental illness and introduced me to a non-profit organization called Project UROK!

Founded in 2014 (launched spring 2015) by 20-something comedian, Jenny Jaffe, their “mission is to create funny, meaningful videos for teenagers struggling with mental health issues, made by people who have been there before.”  They aim to develop an online community to provide teens living with mental illness a sense of hope and belonging. My favorite part of the site, the video section (which I binge watched), has videos by celebrities as well as users. Project UROK! promotes acceptance, empowerment, and changing the conversation about mental illness all things IEI stands firmly behind! 

Can a Cartoon Change How We Think About Mental Illness?

Lindsay Holmes recently brought attention to a cartoon by artist, Robot Hugs, in her piece titled, “What if People Treated Physical Illness Like Mental Illness?,” which was published in the Stronger Together section of the Huffington Post. Titled “Helpful Advice,” the cartoon depicts, in 6 vignettes, what it would be like if we treated physical illness the same way we treat mental illness. My personal favorite being a guy hugging the toilet bowl while another looms over his shoulder saying ” Have you tried…you know… not having the flu?” Holmes says, “many people still don’t get that being diagnosed with a mental illness isn’t something that’s in their control — just like having the flu, or food poisoning, or cancer isn’t in their control.”

See the full article and cartoon here. If you have other cartoons or know other artist whose work focuses on similar topics, please share in the comments section.

*Robot Hugs is a web comic focusing on diverse topics such as mental health, sexuality, and identity.

Oral Health Series Part III: How Oral Healthcare Impacts Vocational Pursuits

This post focuses on how oral healthcare impacts vocational pursuits the last of a three-part series on ORAL HEALTH that began with discussing, the importance of partnering, collaborating and identifying strategies, interventions, and resources to better engage people living with psychiatric disorders about their oral hygiene and Part II how oral healthcare impacts socialization. Based on attending a university colloquium presented by Associate Professor, Dr. Vaishali Singhal called, “Oral Implications of Psychiatric Disorders” I wanted to research more about the vocational implications regarding a lack of oral healthcare not limited to people living with mental illness and/or addiction concerns. While researching I was reminded about a presentation with a colleague on “Wellness and Recovery.”

During the presentation we were informed about a program participant who was receiving pre-vocational services at a partial care program. This person was very active in employment related activities on site, such as identifying work goals, developing a résumé, and practicing interviewing skills. After many months, staff learned that the person was not applying for jobs because he was ashamed and reluctant to mention his missing two front teeth were an emotional, physical, and financial barrier. This article called, “Do missing teeth affect job seekers?” was informative and resourceful. The author Lori Herbert had thoughtfully and empathetically described people’s plight to improve their teeth in a society that seems to usually value physical appearance. Furthermore, she offered potentially reduced dental cost resources to explore in one’s own state. These types of dental circumstances can cause perceived and real challenges of:

  1. Low self esteem
  2. Feeling ashamed
  3. Stigmatized
  4. Isolation and loneliness
  5. Fearfulness

According to a  report from February 29, 2012 called, “Dental Crisis in America/The Need to Expand Access,”  the U.S. Surgeon General’s report, “Oral Health in America,” was cited as stating: students missed 51 million hours of school and employed adults lose more than 164 million hours of work each year due to dental disease or dental visits. I believe you will find the report an insightful read addressing the complexities of accessing oral healthcare for all people and strategies and interventions to help lessen the problem. The U.S. Surgeon General (2000) referred to dental disease as a “silent epidemic.”

What areas of the three-part series on Oral Hygiene did you find most important? Share how you will use these strategies and interventions personally and professionally?

George H. Brice, Jr.

Is a Driver’s License a Dilemma too?

I was talking to a peer who works 30 plus hours a week by getting up at 4:00AM to be on a train by 5:20AM. The person walks to the train station, takes the train, and then connects to a bus. This is a long day- – but more importantly a rewarding routine of earned income, feelings of social inclusion and more. I can empathize as I didn’t drive for 16 years.  I walked and learned to navigate a bus and train in order to work a part time position. I didn’t have to  get up as early as this peer and I applaud them and others who acknowledge the importance and value of employment in one’s recovery journey.

When speaking to this person I was reminded of a provider’s concerns last year about promoting driver’s licenses for people living with mental health concerns. That well-meaning provider and others are concerned about the potential stress put on people with psychiatric conditions to have an expectation of getting a driver’s license.  As I mentioned, I didn’t drive for 16 years, though I actually had a driver’s license.  I lost confidence in driving becoming both vocationally and socially limited. However, I am glad I continued to renew the license which gave me respected and non-stigmatizing identification. Fondly, I remember a friend who moved to Florida giving me round-trip tickets to visit because I earned my Bachelor’s degree in Social Work. I took airport transportation with my “undisputed” driver’s license for airport security check-in. No need for a state issued “non-driver’s licensed” ID. I have now been driving for 10 years affording me expanded work/career opportunities.

So what do you think about persons living with mental illness getting a driver’s license and managing the responsibilities that come with it like anyone else (drive to help out, an emergency situation, ID., etc.)?

George Brice

When the System Works Against Medication Adherence

Between 2004 and 2005, while serving as the Vice-Chairman (mental health consumer representative) on the New Jersey Governor’s Task Force on Mental Health, I had extreme difficulty seeing a psychiatrist. Ironically, this occurred when the task force was discussing Involuntary Outpatient Commitment (IOC) which is now accepted into New Jersey law even though it was strongly opposed by advocates and psychiatric rehabilitation professionals. I was in my 25th year as a service recipient in the public mental health system. I was working full-time and took the day off to attend the psychiatrist appointment. On my way out of a police academy, where I considered renewing my certification as a volunteer certified police instructor, I checked my voicemail to find a message stating: “Your appointment is cancelled today because the psychiatrist can no longer take your health insurance. You will be rescheduled with another staff psychiatrist.” Despite my paraprofessional status and own inferiority complex I went to the agency anyway. After meeting with a person of “authority” I was given permission to see the psychiatrist and thoughtfully informed I would be billed as if I were uninsured. The psychiatrist had no problem seeing me despite the internal agency bureaucracy and I left with my prescriptions. 

Needless to say, I detailed my experience to the task force. About 3 months later I went to see the new psychiatrist, well not really “new” as I had seen that psychiatrist before, but insurance approved. We know psychiatrists are stretched thin and see a lot of people and unfortunately the quality of service sometimes suffers.Nevertheless; when I tried to meet with the new psychiatrist after handing over my co-pay I was informed the psychiatrist was dealing with a crisis and could not give me a time when the psychiatrist would be available: i.e., 15 minutes, 30 minutes or an hour? The expectation was that I would sit and wait. I refused and asked for the prescription to be called in. The response, “we don’t do that.” I left and the psychiatrist called me. I stepped out of my deemed paraprofessional status and inferiority complex as we bantered over the telephone. The psychiatrist reluctantly conceded and called in my prescriptions.

The stigmatizing drama doesn’t stop there as 3 months later, for my next appointment, the same thing happened.  This time the psychiatrist and agency refused to call in my prescriptions, “they don’t do that” and really meant it.

The agency disregarded my time and whether or not I got my medication. However, they were timely mailing me a termination letter as if I were “non-compliant.” The letter failed to state I showed up for my appointments, I paid my copay, and then was told the psychiatrist was unavailable. Despite being in complete distress I advocated elsewhere for a referral. I was given a public system psychiatrist who I could only see if I would “commit” to see a therapist at the agency (see more on shared decision making here). I hadn’t seen a therapist in 3 years. I now figured I was going to lose my job, my career path and my social standing in the community. I was tired!And not going to beg anymore for medication! I’d end up in a state hospital or criminal justice system because of system’s lacking monitoring and oversight.

Fortunately, I got assistance from a friend who put me in touch with a private psychiatrist who even picked up their own phone. After the initial visit with the private psychiatrist I was asked to come back monthly then every 3 months for over a year. Since 2007 I see the psychiatrist every 6 months. Furthermore, I have met courageous individuals, who despite the organ damaging side effects, have relentlessly “adhered” to medication. After 20 years on a medication, I was taken off, as it would have damaged my kidneys. A different medication now processes through my liver.

I believe medication is only a small, often unflattering complex delivery system, and limited aspect of one’s recovery. My recovery is participating in valued social roles beyond the trial and error and limitations of medication. I welcome you to share your own medication experiences; nameless story of a loved one; and as providers your challenges/barriers and resolution ideas to improve medication services so that the system doesn’t impede consumer social roles such as worker, student, and more.

George Brice

A Personal Story

As we work to improve opportunities for people with the lived experience of mental illness, we inevitably find ourselves battling misinformation and prejudice. Whether you’re a peer, a consultant, a provider, a family member, or an educator, you have probably found yourself up against people who have very low expectations for people with mental illness. As vigorously as we challenge those beliefs, nothing is more powerful than a personal story. This link is to an article recently in the New York Times written by a law professor who has a diagnosis of schizophrenia. It is well worth the read.