GOING TO CALIFORNIA STATE PRISON TO MEET TRAVIS by Dede Ranahan

On Sunday, October 14, 2018, I visited with Travis Christian, known to some as BB8099. Travis is an inmate in California State Prison, Sacramento. He’s served five years and has five more to serve. He’s happy to be where he is now compared to where he was a few months ago — in another prison in solitary confinement or the hole. Or the SHU. At first, no books, no paper, no pen, no tv, no radio. Just Travis and four prison walls.

Travis has bipolar/schizo-affective disorder. In a psychotic state, he thought a man was Satan and stabbed him. Hence to prison. In prison, in another psychotic state, he punched a med tech. Hence to solitary. What’s wrong with this picture? When the mental health system doesn’t help someone, and he acts out, we send him to jail. When mental health professionals don’t help him manage his illness, we send him to the hole. Case closed. Hands washed.

This was my first visit to a high security prison. I drove through the wrong entrance and was told. ”You need to back up. The visitor’s entrance is back there.” I asked a question. “No questions. Ask at the Visitors’ Center.”

When I entered the visitors’ admission room, 15 people, from a church group, were ahead of the individuals trying to get in to see their loved ones. It was disorganized. Tempers erupted. “You’re infringing on our visiting time.” When I stepped up to the desk, I was told I needed to fill out a form (that I didn’t know about) and had to leave the line. A woman, visiting her husband, offered to show me the ropes. She helped me purchase a “credit card” to use in the visiting area for the food/drink vending machines.

When Travis’s name was called, I removed my shoes, watch, vest, and glasses to walk through a scanning machine. (Cell phones, combs, lipstick, wallets, and purses are not allowed.) Put back together, I joined a group waiting for a shuttle bus. I wasn’t shy about asking questions — “This is my first visit.” One couple was visiting her brother. He’s due to be released next year and will live with them until he gets his bearings. One woman drives each Sunday from Yuba City (about 43 miles) to visit her son who has schizophrenia. He’s been in prison 22 years. He’s afraid to come out. He believes people will think he’s weird. They won’t understand. Each time a release date is coming up, he does something to get in trouble and to delay his release.

His mom said, “It’s terrible in here. One Sunday three guards played a joke on my son. I couldn’t come to visit that day but they told him he had a visitor. He walked into the visiting area and no one was there for him. The guards laughed. My son was devastated. And they’re making new rules that make things worse.” Who makes the rules? “People in ties and heels sitting around a desk who’ve never been in a prison. Other people, like DJ Jaffe and Pete Earley, have good suggestions but none of them ever get implemented.”

The shuttle arrived and around fifteen of us boarded. The shuttle made stops at different prison entrances (varying levels of security) and the driver called out the names of the prisoners inside. “Christian” was called at the third stop. I got off the bus, walked into a grey, concrete building, and showed my visitor’s pass and my stamped hand to a guard. He opened an electronically locked door. I walked through the door. It closed behind me. A second locked door opened in front of me. I proceeded onto an elevator to Floor 2 and through two more sets of double locked doors. Finally, the visiting area spread wide open. I approached another guard desk to show my visitor’s pass. “Go to table ten and we’ll call the prisoner.”

Fifteen to twenty tables were busy with groups of two or three. I noticed that I was one of two or three white visitors. The rest were African-American or Latino as were most of the inmates. The room was big, square, bleak. Vending machines holding candy, hamburgers, hot dogs, chips, and assorted drinks lined the walls. A red line on the floor marked the perimeter of the room and said, “Out of Bounds.” The microwave area was marked, “Out of Bounds.” People ignored the line to microwave their sandwiches.

I sat down at table ten. I read the rules written on a laminated sheet on the table. One rule was “Face forward at all times.” I faced forward. Another rule was “Keep both hands visible at all times.” And, “The inmate must sit in the center.” (There were three chairs at each table.) And “Keep your feet off the table.” And “Brief hugs/kisses allowed when arriving or leaving.” There were nine rules. I don’t remember the others.

I learned about Travis through this blog. I wrote to him and he wrote back. He was in solitary at the time. Mail was a big deal. I posted his address. I hoped readers would write to him. More about that in a bit.

Travis’s mother, Kathy, sent me photos so I knew what he looked like. I sat waiting at table ten. After about five minutes, I saw him. Travis entered through an opening on the right and walked down a ramp. As he scanned the room, I waved. He spotted me (I’d sent him my photo) and a big smile lit up his face. Our visit, nine months after we first communicated, and one hour after I arrived at the prison, was about to begin.

Tomorrow: Talking with Travis

Travis before prison

Travis before prison

A VISIT WITH TRAVIS by Travis Christian BB8099

Hi Dede,

Sorry about getting back to you so late. I had a mental health crisis and I had to go to the crisis bed. I thought my celly was Satan. I think it’s one of my meds that is causing me this (Abilify). Anyway. Scary.

So Sunday, October 14, would be great for a visit. My mom told me she talked to you.

I am looking forward to our visit. It’s going to be nice to meet a professional author. I am so jazzed about your book and for you and to learn the ropes. I pray for you to get through the process and enjoy it.

Well, I’ll see you soon. If this letter gets there too late that will be a bummer.

Thank you for believing in yourself and setting a good example. I haven’t been writing although, today, I started a journal. It feels good to put my thoughts on paper. Reading has been slow. Still not finished with the book you sent. But I will use it eventually and, hopefully, soon. Thank you. I hope you understand.

I got to go.

Love, Travis

Note: Travis and I have been corresponding since February 2018 but have never met. We will meet, for the first time, when I visit Travis at the California State Prison facility in Represa, California.

See more letters from Travis in the 2018 archives:
February 27, March 14, May 16, June 6, August 22.

Travis

Travis

STAND YOUR GROUND by Mary Irwin Butler

I am both heartbroken and outraged by this story, “I Am Broken. Beyond Repair.” (In the Archives, September 27, 2018). God bless this family. 

I, too, have fought for my son's life four times in the past 16 years — the most recent being this summer. We thought we were losing him again (very similar symptoms as “Broken’s” awful story) from similar medication errors, abrupt discontinuations, multiple sudden changes, and over-medication with horrid combinations of multiple drugs and many injections.

We had to go up against the hospital bureaucracy when attending MDs and nurses began to refuse to communicate with us. At one point, we were "allowed" to get information only through the social worker. We were blacklisted as we watched our son deteriorate mentally and physically. He was a fall risk, could not eat or dress himself, had no short term memory, and had a 24/7 "one on one" aid for a week. It was horrific until we insisted on med changes that took another 2 weeks to bring him around.

Seven years ago my son came down with the rare, and possibly fatal, side effect of Neuroleptic Malignant Syndrome (NMS). For months with severe altered mental status and horrible catatonic symptoms, doctors would not believe us. Finally, an ER physician's assistant recognized, diagnosed, and admitted him to the medical unit, not the psychiatric unit. His suspicions found very labile vitals, fever, and abnormal labs. It was an agonizing nightmare. 

Never give up. Trust your instincts. Stand your ground. Advocate and support your loved ones who cannot speak for themselves. Keep sharing your stories. God bless all.

Mary

Mary

I AM BROKEN. BEYOND REPAIR - An Anonymous Mother

I watched my son suffer a suicide attempt in January 2016. I sat by his side every day. At least he was treated well in Ohio. How I wish we could have stayed there.

In Florida, they Baker Acted (an emergency, involuntary psychiatric examination) him three times. Twice to Gracepoint where he was severely over-medicated. I visited him daily and watched him turn into a zombie. I was on the phone, constantly, advocating and seeking help. Using all my energy for him. His problems consumed my life. I reached out to everyone. In spite of losing myself entirely to try to help him, he’s only received harm and abuse in Florida.

My son was arrested in July 2016. It was a needless arrest that never would have happened had Gracepoint not destroyed his brain and injected him with 400 mg Abilify upon discharge. For two weeks after the injection, he suffered insomnia, severe akathisia, anxiety, paranoia, and hallucinations. He hardly ate or talked and paced the floors day and night.

After his arrest, I went to bed. No longer able to live my life. No longer part of my family’s life. No longer in my granddaughters’ lives. No longer able to function. Because my son suffered, I suffered. I lost everything. I spent the only energy I had advocating and visiting him in jail, or talking with him daily on the phone.  

He’s in worse shape, today, due to all the trauma he’s suffered by the hands of those who call themselves healers. Why are they even in the business? It’s pure corruption here in Florida.

Now, it’s Boley housing and St. Anthony’s Hospital. No parent should have to watch his/her son suffer at the hands or such tormentors. How can they call themselves healthcare professionals or even doctors? All they did was harm him. From 7/26/18 to 8/8/18 he was living in pure hell — a torture chamber. It was completely unnecessary. Didn’t need to happen. Again, I had to exhume some sort of strength to try to advocate and be there every day. It was futile. I couldn’t stop the abuse. 

The week of 7/20/18, my son was cut off 500 mg Clozapine. Cold turkey. Boley did nothing to help him. Boley Baker Acted him on 7/26/18 and the hospital cut off the 225 mg Effexor. Cold turkey. The same day, he was given a forced injection of Geodon/Ativan. On 7/27 he was given a forced injection of Haldol/Ativan. On 7/28 he was given a forced injection of Zyprexa/Ativan and left alone in isolation to suffer seizures all day long. The nurse said he was just attempting to choke himself. She said he was spitting on the med techs. No, he was trying to talk. White foam flew out of his mouth as he tried to speak but only could groan. This is inhumane.

At 5:30 P.M., my husband, Vince, and I arrived for visitation at the psych unit. An RN sat with us to explain that our son was “in crisis” and she couldn’t bring him out to the cafeteria in his condition for a visitation. She mentioned she’d considered a private room for our visitation but didn’t think I’d be able to handle it. I said, “I can handle it.”

She asked, “Do you hear that person screaming?”

I responded, “I don’t hear screaming, I hear someone groaning.”

She stated that our son was groaning, that he’d been in isolation, and needed to remain there. I insisted we see him. When we walked into the TV room, our son was seated in a chair surrounded by med techs. His body was rigid, his jaw clenched, his back arched, his head thrown back with eyes rolling back in his head, and white foam was pouring out of his mouth. Every time he struggled to breathe, I heard gurgling sounds. I touched his hand and he grabbed mine. He tried to turn towards me and speak. His lips moved with his jaw clenched tightly shut. Only groaning noises were coming out along with a lot of white foam. 

One med tech had to stand in front of him with a towel, constantly wiping up the white foam. The white of his right eye started bleeding in 2 areas, filling his eye with blood. I asked what was happening. Everyone stood there wide-eyed. Then the RN told me I had to leave. I said, “No! My son needs immediate medical attention!” I feared for his life. She told me she would get an ICU nurse to assess him. She returned with the ICU nurse and we had to leave. Our son was immediately transported to the CV-ICU unit. I was thinking that the saliva he’d been producing since early morning was actually seizure activity and was concerned about brain damage. 

Around 6:00 P.M., in the CV-ICU, a Bi-pap machine was applied to help our son breathe. He was sedated with an IV drip of Precedex and PRN Ativan. The next day he was transferred back to 6th floor medical unit. Vince and I stayed with him all day.  He couldn’t open his eyes, talk, or feed himself. Nurses began administering oral insulin. They asked us, “Has your son always had diabetes?” We answered, “No, never.”

None of us would escape all that unscathed, but my son had to endure 11 more days of suffering — time in restraints and more drugging — even Thorazine. All he needed was his Clozapine. This is all harm to the patient. Oh, but wait, he’s not a patient. He’s a consumer. Oh, so that’s how they get away from the Hippocratic oath. He’s just a consumer — not a patient — not even a person with the right to “life, liberty and the pursuit of happiness.”

People continue to turn their heads in apathy and indifference while there is an American holocaust going on. No one will speak up. I’m not a doctor. I’m not an attorney. I’m a nobody. Despite all my efforts, my son keeps receiving abuse from the mental harm system. It’s not healthcare.

I am broken. Beyond repair.

Photo credit: josef.stuefer/flickr

Photo credit: josef.stuefer/flickr