THE WAY SOCIETY TEACHES US TO THINK ABOUT SMI IS WRONG by Nikki Landis

Nikki and Kevin

Nikki and Kevin

Another hospitalization. Please keep us in your prayers. 

I always question how much I want to put out there, but not talking about it reinforces stigma. Kevin's brain isn't working right. It's just another organ, folks, with a disease just like diabetes or heart disease. Unfortunately years of stigma and the "mental illness" myth has severely impacted research and treatment. 

Does our society allow 80-year-old patients with dementia decide they don't want to take their meds and live on the street? Or do we make sure they have a warm bed, a roof, food, clothing, and medications? There is almost no difference in symptoms between someone with serious mental illness (SMI) and someone with dementia/Alzheimer's. But nobody says, "He has the right to be homeless and refuse medication" about someone with dementia. 

Someone with heart disease isn't accused of being heartless. Everyone recognizes the heart that pumps our blood isn't the same thing as the heart we fall in love with. When a brain is sick, it isn't the same as the mind. Kevin's mind is still in there. It may not be able to control his brain malfunctioning, but it is completely separate from his actual brain. 

We call it mental illness, but it does a great disservice to the patients. Their mind, the part that loves and cares and wants to be happy, is still in there. There are many disease processes that affect thinking that aren't stigmatized. Yet I know dozens of families that are going through heartbreaking situations with SMI in their families and are scared to talk about it. 

I've never seen the fear of Parkinson's patients that I see of mentally ill patients. How many people know that Schizophrenia and Parkinson's disease are the same disease process? Hypoglycemia is to Diabetes what Parkinson's is to Schizophrenia. Simply different sides of the same coin. Over 50% of Parkinson's patients experience psychosis.

So while Kevin is in the hospital fighting a sickness that is trying to take his life, please take the time to look differently at the woman in the mall having a conversation with herself. Or the man pushing the shopping cart down the street that hasn't showered in a week. They are absolutely no different from the dementia patient in a care facility, or the Parkinson's patient in a warm bed, except that our society doesn't see them. Our society gives them "the right" to live on the streets hungry and alone. 

And don't forget the veterans who risked their lives, many of them giving everything except their lives, who have been left to fend for themselves by a government that signed a contract to take care of them. There are thousands of veterans being mistreated in "Behavioral Health Units" at VA hospitals across the country. As long as our government (and every single one of us that has a voice) allow the VA to even say the phrase "Behavioral Health" in regards to our veterans with brain diseases stemming from chemicals, burn pits, controversial medication practices, PTSD, military sexual assault (which is rampant, people), we are allowing the mistreatment to continue. 

I can't change the world. But maybe, as I sit here looking at my beautiful children who love their father despite his brain not working correctly, I can get a few people to change the way they look at things. The way society teaches us to think about SMI is wrong. The seriously mentally ill (neuropsychological disease, brain disease), are not happy living as though they don't matter. That's a lie everyone tells themselves so they can keep ignoring the problem. People with SMI have families who love them and have tried to move mountains to help them. There are laws to protect their "right to be sick," even though society wouldn't allow someone with any other disease process that significantly impairs thinking to exercise that "right."

MORE FEEDBACK FOR A MOTHER'S DIARY by Dede Ranahan

I have so enjoyed all "sooner than tomorrow" posts. Today's diary post mesmerized me. I loved Patrick's discussion about the poetry of our lives. I was touched by each and every paragraph of today's post.  J.A.

QUESTION:
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ANSWER:
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You are a stunning writer. Understatement makes many times more horrible. Awesome - awful, real, deep...must read. Must subscribe. Beyond heartbreaking, my friend.  Swannie.

 

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COMING UP THURSDAY, SEPTEMBER 21, 2017:  FALL 2013

Fall is an earnest season. In fall, nature reflects on itself and summons acceptance.
Dede Ranahan

"From California" by Gary Thompson
On John Muir's Trail
Bear Star Press 1999
For Patrick Ranahan

SEPTEMBER 18, 2013 - OCTOBER 1, 2013: Aging Can Wait * Real Change in the Air * Who's on First? * Silence * Old and Cranky * Off * Helena * A Pleasant Day * Today's News/Tomorrow's Rewrite * Before and After * Odds and Ends * Worth a Try * Too Much Fun

Pat and me 1969

Pat and me 1969

MORE STORIES FROM ACROSS THE USA - A COMPOSITE

Comments in response to Teresa Pasquini’s “Shattering Silence” campaign (https://www.change.org/p/mary-gilberti-and-nami-board-of-directors-join-families-advocates-of-the-4-in-shattering-silence-about-serious-mental-illness).  2017

"My son has schizophrenia. He committed a very violent crime that was totally out of character for him. That was when he was twenty. He was found not guilty by reason of insanity. The court forced him into treatment for 6 years and then released him home. He refused to take his medicine and slowly but gradually became more violent at home to the point that he was arrested for beating up his older brother. Since then, he has been jailed numerous times for breaking our order of protection we had to take out.

"When he is on his medicine, he is nearly back to normal. Laughing, helpful around the house, and he is social. However, he does not think he is sick and will take his meds for a while but then quits. Then the spiral begins again. He is on the streets now unless he is back in jail. He needs treatment and not jail.

"The patient's civil rights should not include people with a serious mental illness. He has been judged by the social security administration as unemployable due to his illness. That alone should be enough to force treatment or assist in his treatment in a half-way house setting once a person like him is stabilized."  TENNESSEE

"Stray animals are treated better than people. We see a dirty, disoriented animal and prompt action is taken to heal it's wounds and provide a warm safe place to heal emotion and physical wounds.

"Humans though... My brother, languishing in severe delusion and hallucinations (but civil rights intact), died behind a dumpster, not too far from Disneyland, the Happiest Place on Earth. No one seemed to even acknowledge him. He was among the 4% of severely mentally ill people whom are considered "blight" and are criminalized in a misguided belief that it is a US citizen's born right to be sick and die from torment of a brain illness after bouncing from streets to jails to hospitals to streets again. WE NEED CHANGE!"   CALIFORNIA

"My brother is in prison, he has mental illness and is delusional. Seven years in prison has made him much worse. He will come out in three years and be 60 without a penny to his name. Intervention could have kept him an active part of society. As a family we tried but were unable to keep him out of harms way." NEW YORK

"My family member has been immensely helped by Assisted Outpatient Treatment (AOT) and Assertive Community Treat (ACT) team providers. Preventing our family members from further brain damage, by using AOT to assist in their care when they cannot recognize their illness, is humane and required if you love them. Ignoring symptoms of relapse only until AOT is a last resort is unconscionable for us as a society and unforgivable for us as family.

"I receive phone calls from families seeking advice because they didn't know about AOT and their ill family member ended up lost or in prison or worse, dead. This is the reality of mental illness that those who talk about "recovery for everyone" ignore. Not everyone experiences mental illness the same way and not all methods of treatment work for everyone. I support all of us working together but do not support exclusion of the sickest among us, nor do I support using already scarce funds for programs and organizations that are working to the detriment of medicine and scientifically proven evidence-based programs.  Families need to be heard. KENTUCKY

To be continued...

Photo credit: Chris Blakeley/Flickr

Photo credit: Chris Blakeley/Flickr

UPDATE ON SHAYLON: IT'S NOT REALLY GOOD NEWS by Laural Fawcett

Okay,  so here we go again on the merry-go-round of horrors. I have an update about Shaylon. It's not really good news. 

Shaylon, my son, has had a number of psychotic episodes which led him to harm himself and others. Severe visual and auditory hallucinations caused him to leave home and end up on the street. He recently spent a year-and-a-half in jail (he was released in June 2017) because he thought a pedestrian passerby was attacking him and trying to set his feet on fire. This occurred in San Francisco where he often ends up when he is hallucinating. For some reason he, and many others like him, are drawn to San Francisco. I kind of don't blame them. It's a pretty nice city to be in.

I just finished my training as an Emergency Medical Technician (EMT). I have a new job but, essentially, I'm homeless and couch surfing until I get into permanent housing somewhere. It's not the easiest thing to do here in the San Francisco Bay Area where my son has been incarcerated and denied appropriate housing and treatment.

In the last couple of weeks, I showed up at Shaylon's two court hearings. (He was picked up for failing a probation check-in.) What a total, farcical, miscarriage of justice and waste of my time except for the precious opportunity to get a glimpse my son. He was medicated but obviously in psychosis and not well.

The judge repeatedly said, "We don't want you here. You don't belong here and you need to stay away from San Francisco." He didn't speak to other criminal defendants, prior to my son, in such a condescending manner. In fact, other defendants were offered programs and assistance. My son was told, "We can't keep monitoring you." My son's probation officer was reassigned and his new probation officer wrote up a travesty of a report asking him to be extradited to Fresno. The courtroom erupted in laughter when the judge said, "Contrary to popular belief, Fresno is not a foreign country so we cannot extradite him." Neither treatment nor acknowledgement of my son's medical diagnosis were offered. Compassion was in short supply but immature snickering and cruel comments were plentiful.

The court told Shaylon to leave the city — permanently — and ordered him to be released to the streets, again, at an unknown time. I was ignored and marginalized even though the public defender tried to alert the court that I was present on my son's behalf as advocate and caregiver. I wasn't allowed to speak.

I had to travel to Fresno that day to finish my old apartment walk-through to end tenancy and get my much needed deposit back. But my needs and my son's needs were not considered.

Now, once again, Shaylon's whereabouts are unknown.

The public defender's department is saying that the probation department is responsible for providing access to treatment and housing services.The probation department is saying that the public defender's department is responsible for providing treatment and housing services. Meanwhile, no treatment or housing services are being provided by either.  Behind the scenes I discuss how to implement said services with my son's prior assigned probation officer. It remains to be seen.

Why are people with neurological brain disorders being incarcerated? Why isn't my son getting treatment for his psychosis?

Medical professionals and others should be asking, "What is the purpose of the health care and mental health care systems?" In my opinion, the purpose of the healthcare system, and this weird, dangling, anomalous part of it called the "mental health care system," is to bring a person to optimal health. That can't be done in the criminal justice system.

Some of the scariest, most dangerous patients I deal with, as an EMT, have dementia or Alzheimer's. They're medically fragile, confused, and unpredictable. They require tremendous amounts of care and resources, and can wreak havoc on the healthcare system and those who try to work with them. We don't let them wander the streets in misery. We don't discriminate against this population the way we do the seriously mentally ill.

I stand alone. I'm indignant about the injustice against a person, with a grave disability, who happens to be my son. The court forces me to abandon him to street-life hell and homelessness. The court is telling Shaylon to disappear. He's being stripped of his humanity.

*See previous blog posts about Shaylon - June 20, 2017; June 26, 2017; July 3, 2017.

 

Shaylon homeless on the street. Photo taken by a friend who later lost track of Shaylon.

Shaylon homeless on the street. Photo taken by a friend who later lost track of Shaylon.

STORIES FROM ACROSS THE USA - A COMPOSITE

Comments in response to Teresa Pasquini’s “Shattering Silence” campaign (https://www.change.org/p/mary-gilberti-and-nami-board-of-directors-join-families-advocates-of-the-4-in-shattering-silence-about-serious-mental-illness). 2017

“My son is in need of mental health treatment, he thinks he is not ill! I will need help getting him off the streets. He is homeless!” FLORIDA

“People with SMI are often incapable of accepting and continuing treatment to make their lives manageable, calm, and stable - for the inflicted as well as their caregivers and the community at large. We need to do everything in our power to assist families help their loved ones by removing barriers to treatment in the name of privacy and rights before the next inevitable, preventable tragedy occurs.” CALIFORNIA

“I love someone with schizophrenia. He was mandated to Assisted Out Patient Treatment (AOT) in 2009 because he attempted to kill himself and was forced to inpatient four times in the year. He was DX in January. With AOT he went into a half way house for nine months. He became stable and started to live his life. He graduated with honors with a BA in management, works, drives, has an awesome sense of humor, and is starting a peer mentoring program. He will apply to get his Master's degree in counseling and human services next fall. He could have done none of this without the support of his AOT team. The treatment model for people with psychotic illnesses is very flawed. The more support they get to stay stable the better outcome for their life. If they are delusional they can't make rational decisions. Please support AOT.”  CALIFORNIA

“Recently, my adult family member took his life though we tried for nearly a year to get help for him. He had complete lack of insight about his condition and thought he could not die. His neighbors even called the police to report his dangerous (to himself) behavior and we called them and the local mental health department to see how we could get help. We were blocked by the current laws and criteria that make it almost impossible to get help for someone who says they're ok, even when multiple people are reporting and trying desperately to get them help. This was deadly for our family member and traumatic for our entire family. No family or person should suffer this way! It is too late for our loved one, but there are so many more precious lives that could be saved if progress could be made. Every person you see out there on the street (or wherever) is someone's child, sibling or parent. Please help by passing and implementing measures that will help the most vulnerable in our society and their families.”  COLORADO

"I agree that those who have anosognosia, and do not realize they have a mental illness or refuse to take meds, are left to their own devices because, in spite of being mentally ill, their civil rights are more important than their brain disorder. So they can't be forced to take medication against their will.”  PENNSYLVANIA

“I had an older sister who desperately needed help and did not get it. She died alone, without family and homeless."  NEW YORK

“My family has suffered greatly because of severe mental illness of family members: my deceased husband, my son and my sister-in-law. Now my husband and his brother are dead and my son accused. Help stop the pain and suffering families who are unable to get the treatment their love ones need, even when they themselves don't believe it to be so.”  NEW YORK

“As a family member, directly involved in the care of someone released over 50 times without AOT, I know it just doesn't work. Now with just one AOT involvement, my family member has had zero forced hospitalizations in over 6 years. AOT works. Stop the pain and destruction of lives, so advocate for those too seriously ill to help themselves. AOT for SMI Works!”  WISCONSIN

To Be Continued...

Photo credit: Christine/Flickr 

Photo credit: Christine/Flickr

 

LETTER TO HHS INTERDEPARTMENTAL SERIOUS MENTAL ILLNESS COORDINATING COMMITTEE - Jeanne Gore, Teresa Pasquini, Dede Ranahan and 36 Co-signers

This letter was presented at the committee's opening meeting (8/31/2017).

Dear Members of the US DEPARTMENT OF HEALTH AND HUMAN SERVICES INTERDEPARTMENTAL SERIOUS MENTAL ILLNESS COORDINATING COMMITTEE:

We, family members of the 4% who have a serious mental illness, would respectfully like the opportunity to supply you with a rebuttal to Elyn Saks' article, “CONSENT DILEMMA: It’s hard to keep mental-health patients on their medications. Would it help to let them say 'no?'" published in Politico on August 9, 2017.

We’d also like to respectfully remind you the reason the US Department of Health and Human Services Interdepartmental Serious Mental Illness Coordinating Committee exists is that we, the family members of the 4%, along with Representative Timothy Murphy, Representative Eddie Bernice Johnson and her 206 fellow cosponsors of the “Helping Families in Mental Health Crisis Act,” decided to speak out and get real about serious mental illness and the horrific suffering, death, and criminalization of our loved ones.

Please read the gut-wrenching comments (attached) sent in to Teresa Pasquini’s “Shattering Silence” campaign (https://www.change.org/p/mary-gilberti-and-nami-board-of-directors-join-families-advocates-of-the-4-in-shattering-silence-about-serious-mental-illness). You’ll see that many of our loved ones are homeless, jailed, tortured in solitary confinement, committing suicide, and being brought out of prison in body bags. 

Approximately 50% of individuals with schizophrenia, and 40% with bipolar disorder have symptoms of anosognosia, or a lack of insight into their illness. Anosognosia is the single largest reason why people with schizophrenia and bipolar disorder refuse medication or do not seek treatment at all. 

We acknowledge that, with treatment, some people are able to regain insight into their illness and accept treatment. However, as many as 50% of those with schizophrenia and bipolar disorder never do. 

One example of the 50% who don’t ever regain insight is Jeanne Gore’s son. He has schizoaffective disorder and has been hospitalized 43 times over the past 13 years. All but one of those hospitalizations was involuntary because he has no awareness of his illness. He’s been jailed twice, homeless, missing, and beaten up by police and members of the community. When Jeanne got AOT legislation passed in Maine, she was finally able to see her son living successfully in the community. He’s an artist and a musician with a brilliant mind and a generous heart who is now in his own apartment living a good life. As long as he has a court order for treatment, he’ll continue to take medication, all the while insisting that he does not have a mental illness. 

Joy Torres, who suffers from schizophrenia, is a consumer and a family member with children who also have schizophrenia. She says,”Being forced to take my medication saves me and all around me. Not being forced would be life threatening.”

Let’s look at the facts:

Prevalence and Treatment Rates*

  • 8.1 million adults with schizophrenia or bipolar disorder mental illness (3.3% of the population)+
          5.4 million — approximate number with severe bipolar disorder (2.2% of the population), 51% untreated+
          2.7 million — approximate number with schizophrenia (1.1% of the population), 40% untreated+
  • 3.9 million — approximate number untreated in any given year (1.6% of the population)+

Consequences of Non-treatment* 

  • 169,000 homeless people with serious mental illness**
  • 383,000 inmates with mental illness in jails and prisons
  • 50% — estimated percentage of individuals with schizophrenia or bipolar who attempt suicide during their lifetimes
  • 10% — estimated percentage of homicides involving an offender with serious mental illness
    (approximately 1,425 per year at 2014 homicide rates)
  • 29% — estimated percentage of family homicides associated with serious mental illness
  • 50% — estimated percentage of mass killings associated with serious mental illness

* Numbers and percentages of US adults
+National Institute of Mental Health, 2016
**2015 Annual Homeless Assessment Report

Would you deny treatment to someone who suffered a stroke, was having a heart attack, had Alzheimer’s disease or was otherwise incapacitated?  No. We argue that not treating those who are too sick to consent to treatment carries the potential of much greater harm than giving involuntary or, better yet, nonvoluntary treatment. 

Dominic Sisti, PhD, an assistant professor of Medical Ethics & Health Policy at the Perelman School of Medicine at the University of Pennsylvania, recently proposed a new category for psychiatric patients to justify instances of compulsory treatment.

"The current strict limitations on involuntary treatment risk allowing people with psychiatric illness to go untreated and experience worsening symptoms despite compelling evidence that they would want to be well," said Sisti. "A patient may have previously expressed a wish to be treated while in crisis—in which case, a treatment framed as involuntary is actually something else. The proposed concept of nonvoluntary treatment provides a more precise categorization of such cases."

Patients covered by this concept would include those who have expressly indicated a desire to be treated when needed, those who have been living successfully in recovery from mental illness and clearly wish to continue doing so, and those who have difficulty escaping severe drug addiction despite an evident wish to become addiction-free.

The "nonvoluntary" category could also cover patients presenting with their first psychotic episode—due to undiagnosed schizophrenia or bipolar disorder, for example—who essentially have no idea what is happening to them.

The evidence to justify nonvoluntary treatment could include advance directives already provided by the patient to caregivers, as well as testimony from family members, case managers, and primary caregivers — and even the patient's own social media posts.

The nonvoluntary treatment concept would still involve a degree of ethical risk, as the evidence of a patient's authentic wishes might be ambiguous. “But,” Sisti said, “this challenge is not much different from those found in other areas of medicine where a patient seems incapacitated and caregivers and family members must use their own judgment concerning patient care. Moreover, there is potentially much greater harm in not treating these very sick patients compared to providing nonvoluntary treatment.”

In conclusion, we’re promulgating making it easier, rather than harder, to access appropriate treatment and care.  Please reply and continue this discussion with us. We’d appreciate hearing your thoughts about 1) Treating those who are too sick to consent to treatment; 2) A nonvoluntary treatment concept.

Thank you for your service.

 Respectfully Submitted,

Jeanne Gore, advocate, mother of someone with a serious mental illness, President, Families for Treatment of Serious Mental Illness, “We Are Their Voices”  https://www.youtube.com/watch?v=Khbkifi47Ig http://www.treatsmi.org

Teresa Pasquini, Recovering Angry Mom & Co-Founder Mental Illness FACTS, Family and Consumer True Stories

Dede Ranahan, soonerthantomorrow.com A Safe Place to Talk About Mental Illness in Our Families

 Co-signers:

 Joy Torres, mother and someone with a severe MENTAL illness not a simple mental health issue, Chair of Membership, Families for Treatment of Serious Mental Illness

 Mary Murphy, a mother in Springfield Oregon

 Candy DeWitt, Voices of Mothers and Others

 Martie Rhoden Bessler, Mother and Advocate for son and others with SM

 Ray and Connie Maternick, parents of a son who struggles with SMI

 Laura Pogliano, Director, Parents For Care, Baltimore, MD

 Kathy Day, MPA, family member of 25 year old with treatment-resistant paranoid schizophrenia

Cheri VanSant, mother to adult son with bipolar disorder with psychosis in mania/anosognosia. Only after involuntary treatment was my child stable long enough to stay out of a hospital for the last two years. It took 18 years with a lot of lost cognition to make that happen. 18 lost years.

Ruth Medina, M.S. Rehabilitation Counseling, sibling of person with mental illness

Anne Francisco, bereaved mother of son who deserved treatment but got incarceration and  death

Wendy Brown, mother of a son with bipolar with psychosis and OCD

Sandra Turner, Mother of 23 year old Son who desperately sought treatment in Plattsburgh NY, was Sent Away, and dove headfirst into a freight train less than two hours later

 Diann King, a family member of a loved one with a brain disease

 Marcie Sohara, mother to a beloved son with a brain disease

 Lisa Powell, a family member of a loved one with SMI

 Dan West, Father of a son with a brain disorder

 Kimberlee West, Mother of a son with a brain disorder. Also Sister of a smi brother who committed suicide

 Laurie S. Turley, family member of a loved one with serious mental illness

 Kenneth O. Turley, family member of a loved one with serious mental illness

 Roseann Pruett, Mother of twins and widow of SMI

 Angie Geyser, mother and advocate for child with SMI

 Alison Monroe, mother of a dual-diagnosis person with schizophrenia

 Nina McDaniel, mother and advocate for Son with Schizophrenia from Oley, PA

 Janet Hays, President – Healing Minds NOLA

Amanda Woodward, PMHRN-BC, advocate for the seriously mentally ill

 Sabrina Barton, mother of a child with SMI

 Gloria Hill ,Florida Guardian Advocate, have son with serious psych brain disease

 Anthony and Cynthia Hernandez, TTT.transformingtreatabletragedies.org

 Lynn Nanos, LICSW, Mobile Psychiatric Emergency Clinician

 Sylvia Mascareno Charters, MOMI of Florida, son with bipolar with psychosis

 Susan Inman, family caregiver

 Helen Rees, RN, psychiatric nurse and advocate for the seriously mentally ill

 Heather McKenzie, Mother, Mental illness advocate

 Ruth Johnston, mother of incarcerated schizophrenic son