Statement of Solidarity

To all the other Little Voices:

We are waking up to the abuses of our environment,

We have been told we are bad and crazy,

and we are obedient.

We have acted bad and crazy.

We have screamed to get our voices heard

and we are labelled manic.

We have been disbelieved,

and we are labelled distrusting.

We have learned from infancy that safety is arbitrary,

and we are called paranoid.

We have anticipated punishment and deferred to pretenses,

and we have been punished for being manipulative.

We must fragment ourselves to integrate multiple realities,

and this process is called psychosis.

What do labels mean to you?


Trauma – Thoughts of Revenge #1

I survived the mental health system.

I have been verbally/physically abused by nurses, therapists, ER personnel, psych techs, and obviously psychiatrists. A lot of people have been, but they keep quiet about it. The repercussions of trying to tell a mental health professional that abuse occurs within the psychiatric system are monstrous. I have endured a decade of systematic torture. As a result, I’ve developed the symptoms of PTSD, for which I could never afford therapy. Instead, I process things by writing about them.

Revenge? Or Rebellion?

Feelings of revenge are a natural response to trauma. In a study of 96 individuals with PTSD, the severity and repetition of traumatic thoughts surrounding the traumatic event predicted the severity and repetition of thoughts of revenge. Intrusive thoughts were a better predictor than perception of the perpetrator’s being punished for their actions. (Kunst, 2011).

In other words, it might not matter if the abuser is brought to justice; I’ll still be thinking about getting revenge. Should that keep me from fighting this fight? I think many civil rights movements have begun with trauma, and thoughts of bringing the perpetrators of abuse to justice.

Thoughts of revenge have triggers. I take refuge in learning more about my actual conditions: Juvenile Myoclonic Epilepsy and PTSD as opposed to the diagnoses that have been thrown at me over the years to make me go away: Bipolar Disorder, mania with psychosis, ADD, Generalized Anxiety Disorder, Tourette Syndrome, Dystonic reaction to medications, Borderline Personality Disorder, and of course attention-seeking. Learning the truth, while self-healing and constructive, is triggering. I feel rageful, indignant, hopeless, and empty (uncared for).

Maybe it’s unrealistic to expect compensation for what I’ve been though. But people spill coffee in their own laps and get to sue McDonald’s for it.

Letter sent to a medical malpractice attorney:

I think I have a case for malpractice/medical error with Poudre Valley Health’s ER dept.

I have a history of “mental illness” which has been recently identified as being neurological in origin; i.e. I have Myoclonic Epilepsy. I presented frequently at the ER feeling “confused, shaky, and anxious,” and was even taken to the ER by ambulance for “acute dystonia,” and presented often with suspected Autism. Epilepsy was not suspected and I was treated for “psychiatric” conditions.

When released, I had a seizure while driving and got into a very serious car accident, of which I have no memory. I was given another psychiatric evaluation at the ER and taken to a behavioral unit. Although my car was totaled and I face litigation for the property/bodily injury incurred from this accident, PVH ER records indicate the MVA as “minor with minimal damage to vehicles and no injuries.” I was also convicted of reckless driving.

Is this a case for medical error due to mis-diagnosis?

Could be.

Juvenile Myoclonic Epilepsy

Delays in diagnosis are common, often until a generalized tonic-clonic seizure brings the child to medical attention. Ignoring the myoclonic jerks is commonplace. Suspect JME in any adolescent driver involved in a motor vehicle accident when the driver has no memory of the event, but did not sustain a head injury.

Clinical Pediatric Neurology: A Signs and Symptoms Approach (2009) by Gerald M. Fenichel

Imagine if we had a voice; What would we say?

We Are the Chosen

My partner is in the hospital as a result of her personality disorder.


Why would anyone choose to be in a relationship with someone who has a personality disorder?

You don’t choose a partner based on their deficiencies. I try to see the good in people. I’m trusting and naive and probably a bit of a fixer. But ultimately it came down to love. I’m constantly told to leave, but Jane’s sabotaging behaviors have left her two steps away from being a homeless shopping-cart lady who screams at mice. I know she snapped a month ago when I told her to leave my life for a while so that I could try to start picking up the pieces of my shattered reputation and my lost job and home. She drained my bank accounts and left me with nothing but a tent. I should run for the hills, right? But let me ask you, would you feel good driving down the road and seeing a homeless crazy person talking to plants, and thinking “Wow, we were in love a couple months ago?”


These are the facts of my communications with my “partner” at this time:

  • Nearly every conversation ends in arguments over her denial of sabotaging behavior
  • Her consistent plan is to be miraculously rescued by me or people that know her
  • Any and all attempts I make at establishing boundaries (e.g. don’t enter my home uninvited) are met with defenses, excuses, yelling, crying, and then appeals for pity and compassion, in that order.


So why stay? Why torture myself like this?

We are the girlfriends who are frightened of our partners but are afraid to leave because we fear what will happen to us after we do.   -Out of the Fog

I have a disability that I only recently learned about. I fear for my life; I wonder if I’m going to die soon. I wait days on end, alone, for news of what exactly is wrong with me. A couple of good friends have called to offer condolences, but nobody in my life really “checks in,” or has the energy or time to let me vent about my fears and frustrations. When I told one of my best friends I now have constant seizures, she said, “No big deal – just pop an Adderol and you’ll be fine.”

Jane is the only person who cares enough about me to offer emotional support for the exhaustion, the panic, the anxiety, the sadness, the sense of loss, the restriction of freedom, the isolation, the physical pain, and immobility of epilepsy. It’s not a simple, easy decision to just “let Jane go.”


Just because I can’t leave doesn’t mean I’m happy

We are lonely from inside a relationship.

We have put off taking care of ourselves because of the overwhelming “needs” or demands of our partners. We live in a FOG – full of Fear, Obligation and Guilt.

People on the outside of our relationships often have no idea what we live with. Some of us are constantly torn between trying to protect and heal ourselves, and trying to take care of a demanding partner. Others have decided that they no longer want a relationship but don’t know how to protect themselves on the way out. So many of us have been subjected to years of emotional, verbal, physical and sometimes sexual abuse. Sometimes, the worst scars cannot be seen.

-Out of the Fog

Til’ next time,


She’s not crazy either! Complex Post-Traumatic Stress Disorder

I am SCARY (and I like it)

It’s been an exhausting night, but at least I got to say cool gay-rights stuff like, “Oh, so it’s because we’re not married, isn’t it?” and “I’m her emergency contact, and we have rights!” Since the recent supreme court decision, saying stuff like that actually gets you somewhere in the medical and mental health system. They tried to brush me off a few times, denying she was in their ER. My partner was definitely there, definitely not getting the attention she needed and generally being misunderstood by the entire staff.

Loonies, UNITE!

I said my scary bull-dyke stuff, and they relented and admitted they’d admitted her. The in-charge nurse RELUCTANTLY passed my number on to the staff psychiatrist who evaluated Jane, and he called me around midnight last night. Thank the sweet baby Jesus!

“Her father said she’s been prescribed some medication, and she’s not taking it, is that correct?” He asked me.
Wake up, Vico. Wake up and use your mouth-words.

“Well,” I said, “I’m not really sure what medications she’s supposed to be taking. Her mother and step-father fancy themselves her in-home psychiatrists and entrap her in their home and force her to take a pretty wide variety of pills. I don’t know what she should really be on.”

“Hmm,” said the good Jewish doctor from the Bay Area, “Well, the reason I ask is because her behaviors are indicative of Bipolar Disor-”

“She doesn’t have that.” I interrupted. You see, I’ve been clinically diagnosed (by my partner’s 17 year old little brother) as a “know-it-all” and it seems I just can’t stop compulsively knowing things. It’s very damaging to my relationship with my partner’s parents, whom I will refer to as “Borderline-Personality-Mom (BP Mom) and “Creepy-StepDad-Who-Has-a-Gun”(CreepyGunDad).

“She has Complex Post-Traumatic Stress Disorder,” I explained.

The good doctor wasn’t bitter about being interrupted by the crazy girlfriend, which earned him 5,000,000 super-duper gold star happy points.

“Hmm,” he said, “and why do you think that?”

“Oh just her behavior,” I tried to make my answer sound like it was coming from a source other than my compulsively knowing-things-about-things habit. On the strong chance that he had never heard of Complex PTSD, I wanted to validate the good doctor so he didn’t get his little psychiatric feelings hurt and take out his own incompetence on my partner.

“I understand why you may think she’s manic. But she never has hallucinations, never hears voices. She takes risks, and I think that’s the behavior in question here – she absolutely drives recklessly.”

“Yes, and that’s what we’re concerned about,” said the good doctor.

“Yes, you should be. But the reckless driving isn’t just poor impulse control. She takes risks in order to put herself in a dangerous situation; she recreates the environment of her trauma to re-live it, and to to get a chance to change the outcome.” At this point I heard a loud “BING” sound as the lightbulb over the good doctor’s head suddenly ILLUMINATED!

“Do you know what kind of trauma?” asked the good doctor. Which is good, because that information falls outside of the realm of things generated by my unfortunate and clearly mentally ill mind.

“Yeah, I do,” I told him, and I explained that, despite her chronic psychiatric hospitalizations over the past two years, she has never been asked about her trauma or given any chance to speak about it. I only gave him the details of the formative abuse, i.e. the abuse that occurred in the first five years of her life. The list includes emotional, physical and sexual abuse; long-term and repeated entrapment and imprisonment and torture; slavery and enforced labor; long term objectification; and long-term exposure to crisis.

“Wow. That sounds……that sounds awful,” said the good doctor. And the angry little knot with Jane’s name on it that lives in my solar plexus melted just a tiny bit. I explained to the good doctor that Jane would never co-operate with her parents since they are both “part of the whole PTSD thing.”

“Her mother took her to a child psychologist when she was five, who apparently said Jane was doing fine and that they should never talk about it ever again,” I told him.

“What the hell kind of psychologist is that?” the good doctor politely inquired.

“I don’t know, some shitty therapist in Martinez in the 90’s,” I answered, “Please excuse my language.”

The good doctor agreed with me, and I went on to elaborate about BP Mom and CreepyGunDad’s habit of sweeping things under the rug. Without coming across as completely accusatory (which I am) I tried to gently elucidate their tendencies toward chronic accusations, scapegoating, and gaslighting with poor Jane. “That just sounds horrible,” the good doctor responded, and my Jane-knot gradually untwisted to my great relief. I’m sorry, society, but knowing-it-all just feels so good sometimes. I hadn’t even mentioned BP Mom’s chronic physical battle with [horrible degenerative illness retracted to protect the identity of those involved], and CreepyGun Dad’s habit of convincing BP Mom that all her hospital visits could be avoided if Jane would just stop “stressing everybody out.”

The good hospital with the good nurse-in-charge and the good doctor and the good people had no psychiatric beds for the night. She’s been transferred to a different psychiatric hospital. I’m interested in how this will all play out, since the psychiatric system depends on the isolation of their victim to support their pathological abuse and blaming.

The connection between Jane and I is too strong for them to sever, and besides, I’m a Gemini (a lesbian Gemini).

So, Psychiatry, we meet again.
Only this time I’m not trapped in your torture-machine.
We can do this this easy way or the hard way. My only advice is…don’t make me angry. You won’t like me when I’m angry.


Hothead Paisan by Diane DiMassa

I’m probably not just crazy – Frontal Lobe Epilepsy

When I was two years old, I was chasing my mom around and smashed forehead-first into the thresh-hold of the door. It’s a story that bears a permanent scar, but I otherwise tend to forget about it. Then it occured to me today to look up the symptoms of epilepsy caused by damage to the frontal lobe. This is what I found out.

Frontal Lobe Epilepsy (FLE)

Seizure types resulting from FLE are very characteristic simple partial and complex seizures with secondary generalization. During simple partial seizures, consciousness is preserved; the person is alert, can respond to questions or commands, and can remember what occurred during the seizure. During complex partial seizures, consciousness is altered or lost; the ability to pay attention or respond to questions or commands is thus impaired or lost. Often, there is no memory of what happened during all or part of the complex partial seizure. Generalized (tonic-clonic) seizures affect both sides of the body, involve loss of consciousness, and convulsions. Frontal Lobe Epilepsy seizures may be simple partial or complex partial, or they may spread into other body parts (Jacksonian) or amplify into generalized (secondarily generalized) seizures. Or a combination of all of those seizure types.

FLE is characterized by seizures that begin in one part of the brain and spread laterally to other parts, causing an array of symptoms. They can range anywhere from asymmetric and abnormal body positioning to repetitive vocal outbursts and repetitive jerking movements. Emotional aura’s (particularly fear) is associated with FLE, and in patients with FLE fear is shown strongly on the face, as opposed to TLE seizures in which the fear is internal and not shown. Dystonia is usually the first symptom of FLE, which is defined as sustained muscle contractions that cause twisting and repetitive movements or abnormal postures; these movements tend to go unnoticed at first because they are quite brief and don’t affect consciousness at all.

Other symptoms partial seizures due to FLE, depending on the part of the brain affected by neurological discharge:

Supplementary Motor Area (SMA)

-facial grimacing
-inability to speak (selective mutism)

-complex automatisms such as kicking, pelvic thrusting, finger rubbing, lip smacking, chewing or swallowing. Others may include speech, which may or may not be coherent or sensible.
-Responsiveness is often preserved, but the patient will regain consciousness, often feeling disoriented and with no memory of the incident

Primary Motor Cortex (PMC)

-“Jacksonian” seizure, which looks like twitching in one part of the body which sortof “catches on” to the other parts and spreads.
-Clonic movements (alternate involuntary muscular contraction and relaxation in rapid succession)

Anterior (frontal) regions: 
-motor and vocal agitation similar to that of the SMA and accompanied by emotional feelings, often leading to misdiagnosis of a psychological disorder

Dorsolateral cortex:

-clonic movements
-head turn in direction of damaged area of brain (ipsilateral)
-ipsilateral eye deviation (looking)

-swallowing, salivation, chewing
-Clonic facial movements
-Inability to speak

-person is fearful and has epigastric aura (pain in the solar plexus)

Other facts:

The majority of frontal lobe seizures occur between 2 am and noon. I think it’s also interesting that electronic Vagal Nerve Stimulators (VNS) are supposed to be effective in treating this disorder. VNS is a technique I discovered as a teenager, when I started having little “breathing-attacks,” misdiagnosed as anxiety. I would press on my vagal nerve in the small depression in my collar bone and the attacks would decrease.

Maybe I’ve got some brain damage. Maybe the fancy MRI-gadget with it’s pants-crapping gadolinium contrast will show me that brain damage. Monday’s the day.



A Decade of Systematic Torture – Epilepsy in the Mental Health System

Sempervirens Crisis Facility at Humboldt County Mental Health

I am a decade-long survivor of false imprisonment and abuse in the mental health system. I am reaching out to organizations such as pyschrights and Seth Farber’s mindfreedom after trying and failing to get my story told and recognized in my small community in Northern California.

Teenaged Onset and My First Experiences with Stigma

For the first time since I began showing symptoms in 2003, I am now being seen by a primary care provider for my “unspecified seizure disorder.” I have always known my emotional and behavioral issues have stemmed from something neurological, but as a 13 year old growing up in a small farm community in Colorado, I was never able to specifically ask for help with it. My first symptoms were compulsive breath-taking and hand-twitching. My mother brought me to a local child therapist who told me I was imagining things, and anxious. I found it difficult to talk to the therapist due to my habit of ‘zoning out’ when people talked to me, something I now understand as absence (petit mal) seizures. I was also diagnosed with tourettes, OCD and ADD and struggled in school due to attention deficit.

Since I was told my symptoms were psychogenic, I set about learning to control my facial and body contractions. I hated myself for the times that I couldn’t control it, and became fairly anti-social to hide the symptoms I felt responsible for. My mind gradually split into pieces and I developed problems with rage and suicidality. I cut myself frequently and made my first suicide attempt in 2007 after my hand-twitches and facial tic got so far out of control that I couldn’t handle the self-loathing and embarrassment any more. It was my first experience on 5150 in Humboldt County’s mental health crisis unit (Sempervirens) in California. Since I was a minor, I was locked in a small room with a bed and a camera and an older man who sat near my bed all night. These guards are referred to as “StarGuards,” commissioned from American Star Security Corporation. (This part may be edited out as the evidence is only circumstantial: I have information that StarGuard may be a front for an organized child pornography ring associated with Boy Scouts of America in Martinez, CA. They were fully operational in the early 90’s and I do not know if they are still. Denny Peterson of Stockton School District was probably a major organizer – now a PE teacher who was recently filmed battering one of his students).

In between the suicidal gestures, rage, and general issues in school, I was placed on 5-10 different medications as a teenage including Effexor. Effexor caused severe and consistent myoclonic jerks as well as insane out-of-body experiences and compulsive grabbing movements. As usual with akathesia, I was told it would get better with time. I eventually stopped taking the medications cold turkey when I went into University a second time in 2008.

With the support of my friends in school I was able to live with my symptoms for several years and make progress towards my degree. It was only near the end of my school career that my symptoms started taking over again. I would have severe attacks of abdominal crunching, twitching hands and face, racing/repetetive thoughts and compulsive thoughts of suicide. My memories of these times are hazy, and difficult to bring up due to the trauma I experienced.

Sempervirens: Humboldt County, CA

My best friend brought me to Sempervirens because she wanted me to get help with my suicidal thoughts. These thoughts are incredibly difficult to admit to and even more difficult to admit to their cause, which was humiliation over loss of motor control and difficult controlling my bouts of depressive/obsessive thinking which are related to my absence seizures. At first, they refused to admit me because I didn’t explicitly say I had a plan to kill myself – because I didn’t, I only had recurrent thoughts about it – I knew I wanted to live and that’s why I was asking for help (duh). But they manipulated me into saying I had a plan to kill myself, admitted me to Sempervirens (SV) and from that point I became a “child of the system,” so to speak. I confused the things they made me say with things I actually felt. I was given ridiculous amounts of Lorazepam (benzodiazipenes) which smoothed out my tremor but caused days/weeks-long memory lapses in which I acted totally erratically. The staff at SV gave up even making an effort to get me home after discharging me; I often found myself wandering the streets, 7 miles from home, with no idea where I was and no recollection of how I got there.

Suicide attempt: #2

Eventually I gave up hope too, and didn’t want to end up back at SV, so I took the entire bottle of Lorazepam the doctors had given me. Witnesses (friends, paramedics) say I then tried to walk to my friends house but started having seizures on my neighbors front lawn. EMS was called and I woke up in the ICU several days later to my parents’ faces. I had a catheter and a 1-to-1 babysitter. For some reason I had severe metabolic acidosis and hypokalemia, and the doctors told me I must be bulimic. I explained that that was ridiculous and that worked on two different farms at the time and if I spent all my time throwing up I would pass out or waste away. Obviously they didn’t believe me, and the metabolic issue was never addressed.

My parents, who were vehemently opposed to me going back to SV, had me transferred to St. Helena’s Mental Facility in Vallejo for over a week. There I was forced to undergo severe Benzodiazepine withdrawal with no medical aid except a very small dose of seroquel at night. I remember convulsions

wracking my body for several days, and my heart rate was consistently over 110 (it is usually about 70). I was locked in the “quiet room” with padded walls and a camera until I “calmed down.”

Silver Hill Mental Facility

After Vallejo my parents sent me to Silver Hill mental hospital in Connecticut. At this point the doctors at SV had come to the conclusion that I had Borderline Personality Disorder (BPD) due to my returning to their facility so many times, which they saw as attention seeking. Dialectical Behavior Therapy

(DBT) is the supposed wonder-cure for BPD and so my parents had me committed to Silver hill for a minimum of 30 days. Predictably, the residency program didn’t go well at Silver Hill. While my parents complained constantly about their $30,000 going down the drain, I tried to make sense of having been shipped all the way across the country to “get better,” being placed on SSRI’s, Abilify, and Trazedone and dealing with their akathesia and somnolent effects, and did I mention that Hurricane Sandy hit, which completely wiped out power for the hospital and the entire hospital staff’s homes?

I thought the DBT program was a sham since their therapy program was comprised entirely of AA/NA meetings and “mindfulness activities” like blowing bubbles or drawing pictures. After 28 days my hopelessness and despair grew and I was deemed hazardous to myself yet again and sent to their maximum-security (Acute Care Unit) lockdown facility for another month. I had a bed surrounded by cinderblock walls, a private bathroom fitted with anti-hanging devices and which constantly leaked a putrid feces odor from the toilet. There was a small hallway with a window at the end facing the forest which I spent hours staring out of. There was also a day-room with several tables, a couch, an

exercise bike and a television. This was my prison for over a month. I received even less medical/therapeutic attention than I had before. My treatment consisted of my crazy “doctor”

approaching me for about 5 minutes once every few days to say things like, “so, you still gonna go kill yaself?” I wised up and would insist that I had no suicidal thoughts or plans and just wanted to go home, for the love of god. Her typical answer was, “Yah lyin,’ and ya gonna be stuck hyah forevah.”

Easterners… I wasn’t stuck there forever though. They kicked me out the morning after my insurance refused to keep paying for my stay. That was a six A.M. taxi ride alone to the airport and a six hour flight alone to the airport in my hometown. I walked a mile down the road to where I parked my car two months previous, and it was completely covered in mold.

Jason’s death

I returned from Silver Hill with determination to keep myself out of the system. And I succeeded for a while, held down several good jobs and hung out with friends. My mental health faltered again after my roommate and friend Jason Lovell ( killed himself after getting chewed up and spit out of SV. I found myself cycling in and out of SV again, addicted to Ativan again, and acting pretty maniacally. I once escaped from a hospital ER after taking a handful of benadryl to “make the thoughts stop.” I apparently got also into a car accident I forgot about.

Incarceration & Criminal Charges

Because I had woken up so many times in SV, sometimes tied to the bed with people sneering at me, with no idea how I got there, I came to the conclusion that the people at SV were “after me.” I was so symptomatic I could no longer do my job, and wanted to go to the ER but feared going to a hospital anywhere near SV. So I drove North – I got all the way to Coos Bay, Oregon where I entered the ER and gave them a fake name: Dylan Lovell.

Bay Area Hospital in Coos Bay admitted me to their psychiatric ward, where I refused to eat their food or appear to be “looking for a place to stay” in any way, since I had already received that stigma. At that point I was calling my episodes “brain-seizures” and wanted desperately to tell people what was going on and get help. Unfortunately no one ever approached me to ask why I was there. A doctor came in to tell me that I wasn’t in their medical database and that they knew my name was fake and that I wasn’t cooperating. I had written notes about my brain-seizures and taped them to the wall, hoping someone would read them since I wasn’t given the opportunity to speak.

At 11am on my second day in the hospital, I was approached by the group therapist. She calmly spoke to me about my problems with “reality checking.” She said that I was paranoid in thinking that the police were coming to get me and take me somewhere bad. She said she thought I was hearing voices, even though I never said I was. But she offered to come back at 1pm; I would give her my real name and medical history and in return she would get me some ‘real help.’ We made the pact and the mysterious woman went on lunch break.

At 12 noon, a different nurse came bustling in with my clothes. She threw them on the bed, told me to change and “get out.” The doctor then came in and handed me my discharge papers, on suspicion of being ‘un-cooperative.’ At this point my seizures were severely triggered, and my only response was to walk up and down the halls saying, “they said they would help me,” over and over again. Every time they tried to interrupt, I would say it louder. I never became combative or dangerous. They called the police and had me arrested for trespassing, and I went with them quietly and cooperatively.

I was cuffed, driven to the the Douglas City jail, isolated, booked, and harassed. The officers started throwing nuts and me and on the ground, telling my arresting officer his “nuts were getting away.” They treated me like I was retarded. I later paid a lawyer $1,000 to appear for me in court and I’m not really sure whatever came of those charges. They’re the only charges on my criminal record now besides reckless driving – I’ll explain that in a minute.

After I was released from jail, I drove like an idiot to Roseburg, OR and walked into another ER and collapsed on the floor. I was again taken to the psych ward, admitted to Mercy Medical’s psych ward, and locked in a room with a camera and a table. I crawled onto the table which only had a thin sheet and a pillow, sucked my arms into my shirt and put the pillow over me for warmth. I awoke several hours later to a woman ripping the pillow off me and throwing it against the wall. She was screaming, demanding to know “what the hell are you doing here,” “why did you come here,” and “what kind of stupid-ass name is Dylan Lovely anyway?” The screaming and the desecration of my recently deceased friend’s name caused me to start crying, quietly, on the table, and she screamed “if you don’t stop crying, I’ll strap your ass to the bed and forget about you.” This woman had me imprisoned a full day, and refused to let me call my family. I was finally able to call my father but she kept yanking the phone out of my hand and screaming at my dad about what a “liar” I was, and that I was “hospital surfing, looking for a place to lay the head.” My dad convinced the woman that he may sue if she didn’t change her attitude, and suddenly a different nurse appeared. I was then driven via medical transport to Medford to Hallmark mental health wing, where I stayed for about four days. On the last day, they released me with Propanolol, saying there was “nothing they could do for me.” At least nobody screamed at me there. They put me on a greyhound – still in my scrubs and in shoes they found which were 5 sizes to big and without food. People on the bus joked about me being a nurse, I guess because the hospital scrubs looked like nurse scrubs. One kind man was nice enough to see that I was a patient and bought me some Taco Bell. I left California immediately, got a job as a wilderness guide and began learning about the most important equation for someone with neurological problems:

  1. (trigger=episode=impulse) + compulsive action = hospital
  2. trigger + impulse – action = normal life

Fort Collins Nightmare

My next episode occurred in Fort Collins, CO. After my first season as a wilderness guide I was attempting to move into an apartment in a region that was undergoing severe flooding. All housing was reserved for refugees and I ended up sleep-deprived, hungry, and homeless, but not without money. And so I ended up in the mental health system yet again, this time with repeat visits to Touchstone Mental Health in Fort Collins.

At this point my tremors, shakes, twitching, dementia (confusion) and outbursts of rage were completely uncontrollable. I was living with the stigma of Borderline Personality Disorder, so any attempts to talk about my muscle contractions was met with disapproving looks, accusations, and stacks on stacks of freaking breathing exercises. I went through a severe dystonic reaction to neuroleptics in which my extrapyramidal movements completely crippled me. When the ambulance dropped me off at Poudre Valley Hospital, I was given 1mg Ativan for the reaction and forced to leave. I didn’t want to leave and felt scared and seizure-y, but they pushed me out the door in a hospital gown at one in the morning, again several miles from my home and without transportation. I was also placed on Cogentin, a so-called “anti-tardive dyskinesia” medication for uncontrollable jerks and mouth movements.

Depakote and/or Geodon and/or Ativan caused me to have sudden and frequent absence seizures (petit-mals, staring spells). My tongue and jaw became leaden and uncontrollable and I was experiencing visual flashing and extreme somnolence. I drove to Touchstone to complain about all of these symptoms, and they told me I was “just looking for a place to hang out.” They gave me directions to a homeless shelter and told me to get going. So… I got in my car and drove. I had an absence

seizure and drove directly into oncoming traffic. I don’t remember the car accident, and I don’t remember how I skipped from being in an accident to being in Mountain Crest Behavioral Health for a week afterward. But I’ve read my admission to Poudre Valley ER, and this is the official report:

Cheif Complaint – Patient presents with:

-Psychiatric evaluation

HPI 23 yo WF presents to ED with anxiety after being involved in a minor MVA with minimal damage to vehicle and no injuries. Pt recently admitted to Mountain Crest (10/3/2013). The medications she was prescribed are not helping her currently. She wants to go back to Mountain Crest. She complains of her heart pounding and some mild neck pain.

The truth:

My insurance has payed out over $5,000 in vehicular damage and bodily injury to the two other drivers involved in the accident, and they are currently suing for more due to extensive spinal damage that one victim received. My car was crushed completely on one side, totaled, and dragged directly to the junk yard. I complained constantly of severe, relentless shoulder pain. I said it felt like they were coming out of the sockets, which I imagine they did during the crash.

This made me homeless, jobless, and carless.

After the crash I got an apartment with a nice guy, but still melted in and out of calling suicide hotlines looking for help with stomach contractions and pain (I thought they were panic attacks); they would tell me to go to the ER; I would go to the ER, get screamed at, get 1mg Ativan and be sent away in the

middle of the night. My father often sent the police to my house for random “welfare checks.” which stressed my living situation. I decided to get tested for Autism after taking an online Asperger’s test.

Excerpts from my Autism writeup, NeuroDevelopment Center of Colorado

Vico received inpatient care at Mountain Crest during the course of this evaluation. She reported that she was hospitalized due to “sensory overload” (e.g. overly bothered by noises, lights, confused thinking, and rage. An automobile accident prompted the second hospitalization. Hospital records indicate that she was treated for approximately one week for symptoms of psychotic disorder, mood disorder, and borderline personality disorder). Vico is currently without stable housing and reported that she is unsure she will be able to live “like an adult.”

Vico reported unusual sensory experiences, aggression, rage, confused thinking, headaches, and self-stimulating behaviors (e.g. body rocking, looking at shiny objects). She denied racing thoughts or decreased need for sleep.

Vico was referred to the local community mental health center in Fort Collins post hospitalization. The intake therapist indicated an initial impression of Borderline Personality Disorder due to Vico’s emotionality, anger, and confusion. Records from the last two years from the community mental health center in Pagosa Springs, CO [Axis Mental Health] indicated sporadic mental health treatment. Clinical records indicated that Vico sought an Autism/Asperger’s diagnosis [at Axis] and that her suspiciousness made her treatment difficult.

At the time of intake, Vico was reportedly prescribed Depakote, Ativan, and Geodon.

During the initial intake session, Vico presented as anxious, confused, and disorganized. She expressed distrust of the mental health system. Vico reported that her visit to the local mental health center was challenging. She stated that her medication regimen made her feel confused and likely contributed to the events leading up to her auto accident. Vico reported that the medication rendered her unable to talk clearly to the intake therapist at the mental health center. She stated that she would like to conduct a study of women who have been diagnosed with borderline personality [like me, Vico] and test them for autism spectrum disorder [or other neurological disorders] so that she can publish results in journals [I said good experimental master’s theses are published in journals]. Vico expressed a strong desire to fix the “broken mental health system” and to be an advocate for others. [These were later interpreted as “delusions of gradiosity”]

During the testing sessions, Vico continued to display anxiety and confusion. As she acclimated to the testing environment, she appeared calmer and more focused. Vico became tearful and agitated when discussing her immediate future and expressed anxiety regarding how to secure food and housing. When agitated, she displayed voice and hand tremors, body rocking, desire for comforting objects, and she requested dimmer lighting. When this examiner called the intake therapist at the mental health center to coordinate care, Vico expressed anger towards the mental health center therapist. Although Vico appeared agitated at times, she was respectful towards the examiners in this clinic.

Throughout the evaluation, Vico was talkative and expressive. She sustained attention and was compliant with examiner requests. Vico appeared to put forth her best effort on all tasks. Overall, results are considered a valid reflection of Vico’s neurodevelopmental status.

Intellectual abilities:

The difference between her performance on the Verbal Comprehension Index and the Perceptual Reasoning Index was statistically significant and renders a Full Scale composite inaccurate.

Verbal Comprehension Index: 98th percentile
Visual and spatial reasoning reasoning abilities: 68th percentile
Working memory: 82nd percentile.
Processing speed: 30th percentile

Executive Functioning:

Vico was administered the Wisconsin Card Sorting Test to asses frontal lobe functions such as planning and set-shifting. While she was able to grasp the general concept of this test, she found it challenging to sustain her attention and engaged in self-talk to keep herself focused. (…) Though the process appeared effortful at times, she was able to engage in successful problem-solving strategies. Overall, Vico’s executive functions were assessed within the normal range.

Behavior and Social-Emotional Functioning:

Vico appeared anxious during the administration of the ADOS. She looked down at the table during the majority of the session. Vico spoke rapidly and with a flat intonation. She freely shared a great deal of information regarding her experiences and difficulties. Vico often provided more information than was needed. It was difficult to follow her description of non-routine events as her speech was often tangential.

Vico appeared anxious when asked to engage in creative activities. She was observed to have a slight tremor in her voice and she rocked back and forth slightly during these tasks. These behaviors were most noticeable at the beginning of the session and gradually decreased as Vico acclimated. The majority of her conversation focused on the difficulties that she is currently experiencing. This preoccupation is expected given her current situation. Vico frequently drew on the table with her finger or rubbed her stomach and arms while speaking. This appeared to be a coping mechanism for anxiety as opposed to a ritualized behavior.

Vico reports feeling confused, emotionally labile and angry. She indicated that she has difficulty thinking and concentrating. When in crisis, Vico experiences episodes of impaired judgment and deterioration in reality testing. This may include unusual perceptual experiences, magical thinking, or delusional beliefs.

Impressions and Recommendations

Axis 1: Bipolar I disorder, Most recent episode depressed with mixed featres, with anxious distress, and mood-congruent psychotic features

Axis 5: GAF 30 [Defined as: Behavior is considerably influenced by delusions or hallucinations OR serious impairment in communication or judgment (e.g., sometimes incoherent, acts grossly inappropriately, suicidal preoccupation) OR inability to function in almost all areas (e.g., stays in bed all day; no job, home, or friends).]

Vico has researched Autism Spectrum and raised many good points regarding her own thoughts and behavior during interviews. As we find with other bright adults who have struggled with personal relationships and adaptive skills, it is understandable why she requested we explore this possibility. After completing a comprehensive evaluation; however, it was evident that Vico’s reciprocal social communication, insight into emotional experiences, range of interests and capacity for empathy are more advanced than that of adults on the Autism Spectrum.


I decided to let go of getting a diagnosis for whatever was wrong with me. I moved back to California with some friends January 2014, quit taking pills, and have been suicidal thought-free, med-free, and hospitalization-free since October 2013. I allowed my body to do what it needed to do, which was to seize (myoclonus) every morning for about two hours. I developed methods of anxiety control and continued my career as a wilderness guide.

I started using cigarettes as an emotional crutch in 2014, but I got my degree, thank you very much. I received a Bachelor of Science and performed an Honor’s Thesis complete with experimental field design. Career-wise, I’m well-respected within my field.


On Dec 27, 2014, I fell snowboarding at work and hit the back of my head. My work was demanding and I didn’t go to the ER until around midnight that night. They gave me narcotics and sent me away. A month later, I had my first grand-mal seizure. I collapsed several times before anybody noticed and then fell backwards trying to get on the bus to work in the morning. I seized for several minutes and was transported by ambulance to the ER. Gunnison Valley Hospital in Gunnison, CO apparently contains no doctors who know anything about neurology/seizures, or so they told me. I wasn’t given any medication, treatments, or referrals, and made to walk two miles back to my house. I filed a complaint for negligence, which was reviewed and dismissed.

After the first grand mal, I stopped calling for help when they happened. I had two more this Spring, along with countless absence seizures and persistent myoclonus. I finally quit my job due to the hazard I posed to my clients on July 5, 2015. I went to the Mad River Hospital ER in Arcata, CA on July 29th 2015 and got a patient advocate to help me get attention for my seizures. They immediately confiscated my driver’s license but told me to get myself to a doctor’s appointment on Friday. The “doctor” they referred me to was nurse practitioner Vicki Fowler of Mad River Health Clinic (previously Humboldt Open Door Clinic). She performed some sort of exam where she pressed on my stomach and declared I needed an ultrasound, not EEG’s/MRI’s. She said I was “crazy if I thought I was going to get a referral to a neurologist.” She told me my posture was “horrible,” and that I needed to purchase a book from Amazon called “How to Fix Your Own Neck.” I told her I was unemployed and didn’t have cash for books, and she decided that I was “just looking for pain pills,” and told me to “get the hell out of her office.” Guards were summoned. My current partner tried to speak up for me, but we were both forcibly removed. I then collapsed and had 3 grand mals lasting 5 minutes each on the sidewalk outside of the ER department/Mad River Health Clinic. Doctors and nurses were apparently walking by, unconcerned, and the guards only stood by uncertainly for a while before leaving. Finally, a receptionist from a different clinic came out to offer us some water, and referred me to my current primary care physician.

Where I am now

I am currently supporting myself with savings, using friends for rides to the grocery store and post office. I’m going through the hoops of qualifying for state-sponsored insurance and food stamps. I’m working with the patient advocate to get my $5,000 “mental-health” bill expunged from my record. I’m not taking narcotics, and I’m unable to work. I have an appointment for an MRI but have yet to get accepted as a patient by any neurologist. My lack of a diagnosis makes my family doubtful and unsupportive. I seize for about 4 hours a day in the morning and at night.

I appreciate any feedback you might have on my story, as well as any resources you may know of that I can contact for legal/emotional support. I’m wondering if I have any sort of case for negligence with any of the previously mentioned institutions. I now also suffer from severe PTSD as a result of the trauma I experienced in the hospital, and have never considered going back to the mental health system for support. As a high-functioning and gregarious adult, I have an extensive community of loving friends across several states whom I rely on for emotional support, but I’ve never met anybody with experiences similar to mine. I hope to connect with people who understand.

Thank you for your time.


Sempervirens Psyche Ward in Eureka, CA

sempervirensMy experiences here were also horrific and traumatic – all 15 or so of them. I am gathering information about this place in the hopes of exposing it for its frequent human rights violations. Please send in your stories.


Peace be with you

On today’s Democracy Now a story on “hospital dumping” of houseless people said, “In California, a Los Angeles area psychiatric hospital has admitted to abandoning more than 150 mentally disabled homeless patients in dangerous neighborhoods over a two-year period. College Hospital will pay a $1.6 million penalty under a settlement with city attorneys. So-called “hospital dumping” is believed to be a widespread practice in the United States.

Now here’s a paragraph that says a lot.  There is the abandonment and the dangerousness,  but there is also the psychiatric and the 150 mentally disabled.  Of course there is the “homeless,” and you know if they were houseless they were doped, and because they were doped any neighborhood is dangerous.

It has been a long standing practice to release people who feel they are illegally held against their will. Through the lobbying efforts of pharmaceutical financed…

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