Friday, April 10, 2020

April 10, 1978

In the last century, 42 years ago today, I entered employment with the state of Washington. How is that even possible?  I was 20.  There are things in life that are simply inconceivable.  Ronnie’s dad worked with the fed’s Housing and Urban Development for over 40 years in New York City. I don’t know the exact number.  I wish I did so I could know where I stand in the competition. He retired at 65.

When I started, employees smoked at their desks with ashtrays full.  We didn’t know sexual harassment was illegal.  Jimmy Carter was president.  IBM Selectrics were the most fabulous typewriters ever made.

I’m still hoping not to retire. I’ll pretend I’m a doctor, lawyer, or professor and keep my hand in because I’m a professional. We’ll see how that goes. In the meantime, feel free to celebrate 42 years with me.  I’m a dinosaur. At least, I can say I didn’t work for the profit motive. I’ve been lucky. 

I hope one day soon I can re-enter my physical workplace to resume torturing my coworkers by being a comedic ruffian if not the oldest, most senior state worker in the building. I’m attaching a picture of me, Ronnie, and Alex after just 12 years of state work. I had yet to get gray hair. 

Best to all. 

Joceile 

4.10.2020

Wednesday, April 1, 2020

Confessions of a Prankster

364 days a year, I am honest and forthright. Many call me a straight shooter. They’re misinformed as I’m a gay shooter. Regardless, I can be relied on to tell the truth during 99.9% of the year. (My math cannot be more specific.)

Annually, I plan for enjoying with relish that 365th day of the year when I can lie with abandon. I can fib, make up stories, and misrepresent myself intentionally, willy nilly without remorse. This is that day. A mere pandemic has wrecked my plans. 

Because I know we are all keyed up, subjected to unscrupulous, powerful people the other 364 days, I am volunteering to stand down. Please don’t take this as a generous action. I just don’t want to have my pranksterism spill beyond my 365th day. 

To honor this, I’ve dug up an old poem. It is written in the venerable Barbarian poetry style. 

April 1

This is the past voice from April one
You thought I’d forgot, you son of a gun.

This little poem is to tell you how
I so appreciate you, especially now.
When I need a little time to talk
You listen kindly and don’t tell me to walk.

We all have our meetings and quietly chuckle
Instead of crying and biting our knuckle.

So be happy and celebrate this very fine day
It’s exactly one month before the beginning of May.

Joceile
4/1/2004



Moore Barbarian poetry can be found at:  https://joceilemoore.blogspot.com/


[Don't blame me if your eyes bleed.]

[Picture of April 1 circled on calendar with cat and dog picture.]

Monday, March 23, 2020

Listening to the Technically Challenged

“Is your camera on? Can you see me?”


“I think so.  No, the camera thingy has a line through it.”

“Can you click that?”

“I keep clicking on it but nothing happens.”

“Maybe, we can use What’s Ap.”

“I only use What’s Ap with you.  Doesn’t it just text?”

“No, it has a video link.”

“Okay, let me see if that works?”

“Wait.  I’m loading the Skype app.  Maybe, we can see each other on that.”

“Okay.”

“It wants my user ID.  I have no idea what that is.”

“Do you have FaceTime?”

“I only do that with my daughter.”

“Wait.  I’m looking at my What’s Ap.  I think I can do that.”

“Do that.”

“Okay, call me on What’s Ap.  Oh, you’re calling my phone now...  I’ll answer.”

Quiet for a minute.  “You know I would be freaked out if I wasn’t doing this with you.”

“Wait.  Skype costs money to video chat now?”*

A voice from another room.  “Yes, it costs.  But,  Zoom doesn’t.  Microsoft owns Skype now.”

“What?  It used to be free.”

“I still can’t see you.”

“Why is this so complicated?”

Eventually, the talkers settle for a voice call with thoughts of the video chat put off for another time.  Still, they are working to connect on video.  Forty-five minutes later, success on Skype.

Welcome to social distancing 2020.

L’Chaim.

Joceile

3.23.2020


*Skype doesn’t cost for video chat if you have a Skype account and are not using their phone number.

[Picture of me on FaceTime app.]

Saturday, February 22, 2020

MY RAGE LONG SUPPRESSED

I had my weekly counseling appointment this morning. I’m seeing a new therapist because my previous therapist (beloved) retired. Prior to her departure, she steered me to Stacy who was someone she admired. This process of getting to know a new therapist is not my favorite.  I avoid having to do it by being committed to the person I work with.  There’s not much I can do about retirement.

A by-product of the process of sharing what makes me who I am with a new therapist is encountering new perspectives on the inner turmoil that makes a life.  I shared with her my history of childhood abuse, self-harm, institutionalization, and long, long recovery.  It includes the part of my experience where voices spoke to me in my head and the subsequent making peace with those parts.

One way for her to understand me is to read a book I wrote about the experiences.  It also brings up opportunities for her to ask questions and for me to clarify.  She has an inherent understanding of why childhood trauma (or any severe trauma) might cause dissociation which demonstrates the incredible creativity of the human brain to find ways to survive.

When I talk about being in Child Study and Treatment Center, the youth portion of Western State Hospital, in 1972, it’s hard for people to understand how that experience could be both extremely life affirming and of virtually no therapeutic value.  It got me out of my parents’ houses.  I got to see movies, camp, hike, and ride trains.  I learned I could ask for a hug when I wanted one.  It enabled me to live with my grandparents.  What I did not learn was anything about acknowledging or managing trauma.

In 1972, arm cutting was not on the forefront of media.  There were not dozens of kids in each high school around the country expressing their pain via overt self harm.  It was new to my middle school counselor.  It was new to the school principal.  It was a rarity at Child Study at that time.  It leads us to a conversation about being on the leading edge and born at a time when the issues in my life were not represented around me or in media.

My brother-in-law is an example.  Born in 1955, Philip had severe autism.  It was difficult for the doctors of the day to diagnose.  It was an era where the cause for autistic children was blamed for what specialists called “the refrigerator mom.”  When in doubt, blame the mom. The harm it did to Philip, Ronnie, and her parents is incalculable.  Philip was pulled from his family and placed in a state mental hospital because there were no treatment protocols, support systems, or understanding for how much potential Philip might have.  Had he been born 40 years later, his entire life experience would have been different as would that of Ronnie and her parents.  It was not to be.

Fighting through my experiences on the forefront of what is commonly known by society has been a pattern for me.  I told Stacy about transitioning from female to male and back to female in 1978-79 and working for civil justice and disability rights.  I told her about doing standup comedy in 1986, telling humorous stories about mistaken gender identity.

“The trouble was back then gay audiences were in hysterics.  Straight audiences couldn’t even allow themselves to laugh.  That’s all different now.”

This leads me to my current struggle with virtually undiagnosed neurological difficulties.  Do I have MS, transverse myelitis, idiopathic neuropathy, partridge in a pear tree, or what I euphemistically call “No Walk-us?”  There is no western medicine treatment for what ails me.  The medicines offered only suppress my neurological system.  In talking to people with similar neuro symptoms, it appears that neurological disorders are on a spectrum and many are closely related.  However, western knowledge isn’t there yet.


My personal theory is that my neuro-system has been in a state of over threshold since I was little as I learned to ignore the fear and panic as I was assaulted.  I have been in a physical freeze while my system bleats out an alarm for over 60 years.  I think this is enough to cause a misfire of communication from my nervous system to my brain.

This leads me to acknowledge to my new therapist a simmering, burning inner rage.  It’s a neurological dis-ease based on trauma.  Western medicine does not acknowledge this paradox.  To do so, might cause us to ask why we continue to fail to address trauma of many types.  Why we continue to deny generational trauma when the evidence is everywhere around us.

These last few months I worked with a veteran who was in the army for 27 years.  He survived nine deployments without serious injury.  A year ago, he had a motorcycle accident which seriously messed up his shoulder.  He said, “Nine deployments and I get taken out by my bike.”  He shook his head.

He was full of barely restrained energy.  He was fun and playful.  Even while I enjoyed him, I sensed trouble inside.  He told me his best friend was killed during a deployment last fall.  I told him I was afraid for him.  I sensed his rage was Hot.  “Don’t burn yourself, buddy.”  In frustration, he quit his job two weeks ago.  I said, “Don’t put yourself in harms way.”  He suggested he had a friend that was hooking him up with a contract back in the middle east.  When the fire is too hot, life gets cheap.  I can’t save him.  I can only send him love.  I suspect I’ll never see him again.

Inner rage: some are aware of it. Women friends, African American friends, Jewish friends,  disenfranchised of many types—people who experience both individual and societal harm not for what they’ve done but merely for who they are and the value our society places on us, seeing us as “them.”

Starting at three or younger, I was subjected to years and years of abuse, sexual, physical, and emotional, because I was my father’s property. He could treat me however he liked, hit me, assault me, and all the while proclaiming it his absolute right.  By intimidation, instilling fear, and far superior strength, he could enforce his fiefdom on our family.

Once after he had beat me with a belt, including the dog within an inch of his life, my mother took all the belts out of the house to her parent’s house.  His response, “Bring them back or I’ll use one on you!”  She brought them back the next day.  He beat me, insisting he would continue until I cried.  I wouldn’t cry.  That holding in harmed me.

Being subordinated to a man who uses his power this way, who said with no trace of humor, “I brought you into this world, I’ll take you out,” I learned the freeze part of flight, fight, or freeze.  Freeze was the only life protective resource I had.  When a deadly animal has you in its sights, do not move.  Don’t give it something to chase.  Don’t give it something to fight.  Appear to not pose a threat.  If it’s not too hungry, you may survive.  My father was such an animal.  In freezing, I survived but not without cost.

When I talk to my therapist about my long, long road to life sustaining mental health, the other side of the coin is how trauma and abuse has hurt my body.  My neurological system is in an uproar.  Often nerves don’t communicate well leading to altered motor skills and sensations.  Western medicine has nothing definitive and loves to say I’m not trying hard enough.  It’s hard for me to resist agreeing.

When I explain the dynamic that after mental health it’s the body’s turn, I believe I know that the neurological damage is in part a result of sustained mental and physical trauma.  If during my formative years I suppressed this global frozen rage towards my father and to some degree my mother, it has inhabited my body on a cellular level (and I’m not talking AT&T here).

Those very cells that resonate and sing out with universal connection when I see an enchanting sunrise or trees that go to the horizon are the same ones that contain the anger of hundreds of atomic bombs because the rage has gotten down to my atomic level.

It begs the question, “What does one do with atomic rage?”  There are thousands of answers.  With rage at the cellular, they are not easily followed.  I have to find a way to point it outwards, away from me, and not inside.  It requires a lifetime of practice.  It’s trial and error.  I won’t be done before my time is over.  Listening to Freddie Mercury sing, “Who wants to live forever?” with his soaring voice and impassioned plea, I know no one gets to live forever.  I’m okay with that.  The pointed elegance of life must surely wear down like the stone under flowing water.  The beauty is in the process.  No one owns the end.  Still, the rage burns.

L’Chaim.

Joceile

2.21.2020

[Picture of the male and female nervous system.]

Tuesday, January 28, 2020

The Last Time I Was Hospitalized

There is a short life cycle of a mental patient on a psych ward. There has always been a cycle for me when I get hospitalized for being suicidal. There are a lot of the same people there with individual variations. I recognize the types.  There’s a point where I think, “Ah, I know how to be here.”  It’s happened to me enough times that I think I’ve got it. “Yep, this is how it goes.”  Last night, I had a common dream about being hospitalized and being aware of the cycle. 

The last time I was hospitalized was February 2013. After eight ungodly hours sequestered in St. Peter Hospital’s ER after I hurt myself, I arrived by ambulance.  It’s a long drive from Olympia to Kirkland’s Fairfax Psychiatric Hospital.  

I remember more characters from that hospitalization than usual.  I generally forget the most notable people in a week or two.  This time after being in the hospital for five days, they were etched in my mind so strongly that within a few days I wrote down all the patients’ names I could remember, their ages, and short biographies.  Sixteen patients followed by seven staff members similarly identified, whether they liked their jobs, and if not their life plans. Once I made these lists, I was able to let go of preserving them carefully in my mind. 

When hospitalized, the first thing is to identify staff members I like.  This is basically an assessment of resources. These are the people I will go to to ask for things. Washing clothes, special medication, admission questions, making a phone call. That sort of thing.  

Since my previous hospitalization, psych staff had realized that cell phones violated patient confidentiality.  Therefore, we turned in our phones and shared a community phone.  Patients would answer it and yell the name of who it was for.  Not a particularly confidential methodology.  This also required not hanging on the phone forever to friends and loved ones.  During therapy sessions, the phone was off limits.

The next thing on my agenda was to identify patients I liked. These would be the people to follow around and learn the ropes. This is the best source for learning how meals work.  I follow them, sit with, and get to know them. First making small talk, then gradually going deeper. 

I noticed Pat right off.  She was a pixie sized, British woman who road a Harley.  She was a quick buddy and confidant.

I saw a tall, handsome African American man named Abraham who used a cane. I found out later he’d recently been diagnosed with MS. Feeling like his body let him down, he was struggling with letting go of his identity of being physically strong and a family provider. It flung him into a deep Depression. 

Stacy with long red hair was an RN in an ARNP program who struggled with lifelong Depression.  She was so depressed and suicidal that she could barely function.  She was one of my roommates.  She was walking in a boot for an injured foot. There were three beds to a room. Stacy, me, and Terry.  There’s always a patient or two who barely talks. Terry was like that. I learned there was a more severe unit called “North.”  There are always nicknames for things in wards.  We were in “Central.”  Terry was recently moved from North.  You never ask people why they’re there.  Eventually, most people volunteer.  Silent, Terry remained a mystery to me because she never shared her story. 



There are always a broad range of ages as well as abilities. Some people talk a lot. In fact, so much I wished they’d stop. Others mumble which can include rocking. A finite number communicate fairly normally. Those people easily share their stories. Most of the stories are very sad. This is to be expected. It’s not like we’re at summer camp or in college dorms. 

Every hospital ward has different rules to learn.  I have to make my peace with them. Meals were eaten in the cafeteria three times a day.  We all trooped down a long hall.  I hung close to Pat.  It was after a couple meals I learned that I had to wear shoes to meals.  Because I had neuropathy in my feet, I tended to walk around in my socks.

Due to the neuropathy and the pain medication I take because of it, the first order of business was to get my assigned psychiatrist, Dr. Peters, to approve my prescribed pain medication.  It’s a delicate action that requires a bit of finesse.  I had a legitimate need.  I was not drug seeking.  I told her I would take the least amount possible.  We agreed on one in the morning and one in the late afternoon.  I liked her.  She didn’t waste time but listened well.  I didn’t see her very often once my psych meds were arranged.

We were assigned to groups for group therapy and activities.  Two sessions in the morning; one in the afternoon; and one in the evening.  There were breaks and snacks.  The rest of the time some patients watched television and the rest of us sat around a table coloring pictures with colored pencils.  This was my favorite activity.  Coloring and talking.  It was one place where I learned about fellow patients.  Eventually, I would get clues about what they thought of me. Although, no one ever said a word about the wound on my arm. 

There were regular outdoor breaks in a closed yard.  This was for smokers but most of us availed ourselves of an opportunity to get outside.  It was February in Seattle.  It wasn’t too cold or too wet that week.  It was also an opportunity to talk to staff members I liked as they were chilling outside too.

Across from us in another ward were those recovering from addiction.  We only crossed paths in the cafeteria.  I carefully watched the tone of the staff and patients in the addiction recovery unit.  There was a difference in how the two communities acted.  There was less trust and compassion among the addiction recovery staff and patients.  I detected a certain assumption that everyone was always working an angle.  I might have made this up but I resolved to stick with the craziness business and not get thrown into that group at any point in the future.

Terry barely spoke at all.  I could tell she was very distressed not just in whatever her diagnosis was but something big was on her plate.  She suffered from frequent headaches.  I did learn she was a pitcher on a boy’s baseball team which interested me.  But, that was about all I got.

Stacy, my other roommate, only talked to me at night in the dark while we laid there staring at the ceiling not sleeping.  My bed was in the middle.

“You know how I broke my foot?”  

“No.  How?”

“I walked twenty miles to the ER. I was suicidal.  It took all night.”

“Why did you walk?”  I asked.

“I didn’t want to ask anyone for help.  By the time I got there, my foot had a compression fracture.”

“It’s okay to ask for help, you know?”

“I didn’t want to.”

I felt very sorry for Stacy making that long lonely walk, thinking she didn’t want to ask anyone for a ride.  I felt lucky I had people to ask for help.  I soon learned that what we talked about at night was off limits during the day.  She just wasn’t interested in talking in daylight.  We only had a night time relationship.  It was another marker of her loneliness.  She told me she had only been out of Fairfax for nine days when she had to come back.  The staff hadn’t changed from the first time and treated her kindly.

On the other hand, Pat was a highly entertaining. She was outspoken with that very cute British accent.  She road a hog all over the place and was determined to ride down to see me in Olympia after we got out.  Her diagnosis wasn’t clear to me.  She said she had been diagnosed as Bi-polar for ten years but Fairfax psychiatrists said she had PTSD and Anxiety Disorder.  Married to a gay rancher in Colorado for 15 years, her current husband was an ARNP.  She said she loved being a bureaucrat in London.  I had to wonder just how long ago that was.

I learned more as we colored.  Another woman, Sheila, in her early sixties seemed equally lost.  Her son had brought her there.  Her husband had died in November.  Sadly, he was a drinking alcoholic for twenty-two years of their marriage.  She had kicked him out a year ago.  He finally went to treatment and had died in the detox facility.  They had exactly one month of his sobriety to make amends before he died of liver failure. She was afraid to go home before Valentine’s Day. When she was discharged, she signed up for day treatment consisting of morning sessions at the hospital.

Another night, Stacy talked to me about her history of being suicidal.  She told me about her mother’s long frustration with her struggling with wanting to die.  She said, “Finally, my mother said, ‘Well, if that’s the way it has to be for you to find relief...’”  As a mother, it broke my heart laying in the dark unable to reconcile the inexcusable betrayal of a mother giving permission to her daughter to kill herself.

The next day was the only time I spoke to Stacy during the day about our night time conversation.  I cornered her in the bedroom that afternoon and said, “Stacy, I just want to tell you I thought about what you said.  As a mother, it is never okay for a mother tell her daughter it’s okay to kill herself.  It is never okay.  There’s no excuse.  I could never condone saying that to my daughter.”  Stacy politely nodded that she heard me but said nothing.  I’ve often wondered what happened to Stacy.

For other patients, I actually learned things about them in therapy sessions.  Abraham was 42.  He was diagnosed with MS the year before.  He quickly lost his incredible physical well being and strength.  He was terrified that he could no longer defend himself.  In frustration, he had quit all his doctors, gone into his room at home with the lights off and curtails closed, and just sat for months.  Finally, his wife got him into the hospital.

Coming from North as an involuntary commitment, Terry had freedom restrictions on the ward.  Terry and I had specially locking bedside tables for our CPAP machines which was how we ended up together.  I had never adapted to my CPAP but it was there.  One night, a staff member came in to check on Terry.  She found Terry trying to strangle herself with a towel in our bathroom.  Unobtrusively, I witnessed Terry being taken to a closed room.  She had to surrender her clothes and put on a strange stiff, uncomfortable dark green garment with Velcro closures.  I resolved to avoid that outcome at all costs.

Each morning, I asked staff to get a pain pill.  I learned to do it before breakfast.  Otherwise, the wait could be interminable.  Tom tended to be in charge of medication.  He was the slowest med deliverer I had ever seen.  It took him forever to dole out meds.  It made me crazy (using the term loosely).  While standing in the pharmacy doorway waiting for my medication, he said he’d been there a year and liked his work.  That made one of us.

At 4 p.m., I’d ask for the second pain pill.  It was after shift change and before dinner.  Every day, the staff person would remind me it was my last one for the day.  I wanted to say, “I know that, goddamn it,” but restrained myself.  I surmise they had to operate based on the lowest communication denominator.

I often walked with Samuel to meals because we both walked slow.  At 6’4”, he was a big African American man with an odd gait.  He had been at The Evergreen State College, worked in schools, and hoped to get a state job in Olympia some day.  He was exceptionally kind.  When he was discharged to outpatient treatment, he shook my hand.  I never learned where he lived.  I just liked him.

Naturally in a mental ward, I never know what stories people tell are true.  Carol at 26 said she was a figure skater and had a job offer in Colorado as a coach.  She was on a 72 hour involuntary hold.  She said she started Olympic training when she was young and said her skating was on YouTube.  Her parents came to visit.  It was pretty obvious that her issue was an eating disorder of the not eating enough variety.  She didn’t seem all there literally and figuratively.

Michelle said she worked at Department of Social and Health Services.  I only saw her for two days.  She spent her all of her efforts trying to get a transfer to St. Peter Hospital in Olympia.  She said she felt ignored at Fairfax.  Given that all of her observable efforts were toward getting transferred, it wasn’t surprising she felt ignored while she ignored everyone and everything at Fairfax.

Kimmi was Hawaiian and transgender.  At 30, she was beautiful and fun.  She told me she was an airline attendant, currently working in customer service, and wanted to be a waitress.  I didn’t delve too deeply.  I just enjoyed her sparkle.

We had art classes.  We had various types of group therapy.  The therapy value seems to be just to get people to talk.  In fact, it’s mandatory to take turns talking regardless of the therapy motif.  I have no problem making stuff up to talk about.  It’s painful to watch others struggle to find words.  Usually, they have been trying to fly under the radar.  Eventually, the spotlight turns on them.

Aaron was a tall, well built white man.  As a staffer during gym period, it was obvious he was very athletic.  He could barely restrain himself and had lots of energy.  He had a BA in psychology but looked exactly like an undercover FBI agent.  He was trained as an EMT, wanted to be a firefighter, and was leaving in three weeks for an EMT job.  He and Kimmi played dodgeball.  They were both very muscular and didn’t pull their punches playing against each other.  If they had played with the rest of us, we would have been creamed.

My favorite staff person was Lisa.  As the RN charge nurse, she worked long days.  With long blondish, brown hair, she was very fit and the mother of two boys.  She was bright and very efficient.  If I needed something, she was always my first choice.  She was the one who came and found Terry with the attempted towel suicide.

I had conversations with Linh, a Chinese-Vietnamese American staffer.  At 23, she had a BA in psychology.  She talked about not knowing if she wanted to go into nursing or continue psychological staffing.  As a human resource professional, I’m always interested in people’s jobs and life plans.  She told me she felt parental pressure to be a professional.  I’m always of the “do what you want” frame of mind.  I don’t think that was helpful.

Sitting around the table coloring, Mary was over 50 and said she had lost 170 pounds.  She was a short, round bodied woman who didn’t talk much.  She took a liking to me.  In art class, I made a purple and green bracelet.  She asked me if she could have it because they were her favorite colors.  It was an easy thing to give.  She lived in Everett and needed to move closer to the hospital.  A friend was going to help her find an apartment.  When she learned I was leaving, she hugged me and asked if she could come with me.  I wish I could have helped.



There was one guy in particular that was universally disliked.  Rob was very off balance.  He talked too much and got in people’s faces.  He knew everything about everything including government secrets and was happy to tell us about them.  He was an involuntary patient monitored closely by staff.  

In the psych patient world, there is a significant difference between voluntary and involuntary.  Voluntary meant I could leave any time, possibly against medical advice, but I could leave.  Involuntary meant a patient had been placed there by the court and couldn’t leave until released.  Involuntary may or may not mean something about the severity of the condition.  However, it does mean that there’s probably an ugly story involving outsiders about how they got there.

As Pat and I got to know each other better, we shared more about our lives including our daughters and her granddaughter.  She told me when I came in I looked stiff with my shoulders up around my ears.  That’s pretty much what happens to me when I’m tense.  Ultimately, we shared email addresses and phone numbers.  After discharge, we exchanged a few emails but then she fell off the radar.  I sent her several unanswered emails.  I have no idea what happened to her which is the nature of transitory relationships.  Ronnie calls it “significant relationships with insignificant others.”

Another patient I was curious about was Edmundo or Ed as he preferred to be called.  He was a Mexican American with three boys aged 1 to 11 who also came from North.  He proudly stated he got up at 4:30 every morning, did stretches, and read the Bible for two hours.  He told me he had “peace in his heart.”  I was left wondering why he was there.  I also noticed he wasn’t up early in the morning doing stretches or reading the Bible.  Maybe that was his non-patient schedule. 

As the days passed, I felt more and more like myself.  It was time to leave.  I asked Lisa on the morning of the fifth day if I could go home because I was ready.  She said, “I was wondering when you were going to bring that up.”  Arrangements were made and Ronnie was called.  

Ronnie picked me up late Monday afternoon for the long drive home.  It was a bright, sunny day.  I said my good-byes, refreshed from my psychiatric reboot, ready to re-enter my life.  Because I arrived in an ambulance, I hadn’t seen the outside of the hospital.  I didn’t realize it was an official mental hospital until I saw the sign.  We loaded up my meager belongings in the Prius.

As Ronnie left the parking lot and started driving, I was shocked by the quickly moving traffic and intensity of sights and sounds.  After the slowness and faint boredom of hospital life, the world was busy and overwhelming.  There’s a little fear in getting out tempered by being with my partner, on our way home to see our cat and dog, and being in the world followed later by returning to work.  It’s also a bit joyful remembering what my life is and that I’ve chosen it.  Suicide has not dogged me since.  Still, I never forget that Depression is easily aroused if I fail to attend to self care. 

L’Chaim.

Joceile

1.26.2020

[Names have been changed.  Pictures of Fairfax ward sparse patient beds and seating in day room.]

Saturday, January 4, 2020

Life with DeeBot

Ronnie and I don’t have a smart house nor do we want one. It turns out that little DeeBot is more than we can manage. And, she isn’t even connected to the internet or our phones.  Just a little motorized vacuum that has a mind of its own. 

I got DeeBot for my birthday a year ago. I wanted to have a cleaner house without vacuuming every other day. We have a large long haired dog and small long haired cat.  Both of them go freely inside and out bringing in all sorts of dirtish crap.  I set DeeBot on the floor, press go, and she’s off cleaning and dusting the floor with her vacuum, roller, and little arms awhirling. 

It works for me to have her clean while I do other things.  She does not go down the stairs except for that one time I confused her.  Bump, flip, bump, flip, bump, quiet.  I rescued her and determined she did not have a concussion or traumatic brain injury.  There are a couple places in the house where she stops because she’s confused.  I have to pick up or tuck under rugs with fringes because she can’t tell those fringes are off limits.

The cat, Scarlett, hates vacuums but thinks nothing of DeeBot.  The dog, Sheba, doesn’t mind vacuums but is pretty unnerved by DeeBot running around loose possibly in search of Sheba’s tail.  I block off the bedroom so Sheba can escape.  DeeBot doesn’t do well in the bedroom anyway because we have stuff under the bed that acts like a DeeBot trap.

I run DeeBot when I’m home.  She has a clock and the option to set a schedule but I prefer to be in charge.  I’ve also heard entertaining stories about sibling DeeBots coming up on cat barf or dog accidents and happily spreading them around the house.  

With a remote, she acts like a little remote car.  If we’d had a DeeBot when I was a kid, I’d have been in hog heaven.  Remotes were a big thing then.  Now, we take these remote things for granted.

Watching DeeBot is looking into a computerized mind.  On her basic setting, DeeBot appears to aimlessly cross the floor Willy-nilly in the hopes that if she crosses it enough the whole floor will get clean.  I took a picture of her doing the carpet.  Her process looks like this:


Basic computers do actions without reference to conserving energy or brain power.  Their actions are by “brute force.”  This means that a computer looks for a word by going through the entire dictionary until it finds the word.  Because this looking through the entire dictionary is so fast, humans don’t have to notice what looks to us like the long way around.  DeeBot uses the same method to clean the house.  Going over and over it at odd angles with the idea that eventually it will all get clean.  Humans have a different approach and the computer way can be confounding to us even though it still works.

DeeBot does have a couple settings for going around the edge of the room, turning circles over the same spot, or going back and forth in more or less of a straight line.  She is not connected to the internet so she doesn’t get smarter and smarter about how my house is designed.  I’m more than okay with that.  I have no idea what kind of trouble might find her if she links up with those mobster internet computers.

Ronnie and I both appreciate the house being cleaner.  Ronnie was uncertain about getting DeeBot.  I used the old get-it-for-my-birthday trick.  Ronnie now appreciates DeeBot.  Though, it’s hard for her not to talk to her.  “Hi, DeeBot.”  “Excuse me, DeeBot.”  

I do have to spend five minutes emptying her collection box and cleaning her rollers of accumulated animal hair.  But overall, it is much easier for me than the 20 minutes spent vacuuming.  I can eat or read a book while she does the vacuuming.

A few months ago, DeeBot got it into her head that she should start cleaning every night at 11.  I said, “No, DeeBot.”  But, she didn’t listen.  I broke out the instruction manual which is exceptionally poorly written to determine what was causing her to think this.  It appeared she needed a reboot.  I turned her off.  I pulled out her battery for half an hour.  I inspected her remote for unwanted settings and pulled its battery.  She still woke up at 11 at night and started cleaning.

I emailed the DeeBot company.  A formulated computerized response confirmed the rebooting procedures.  I went through all the above again.  When she still woke herself up, I emailed them again.  We went through all the procedures again from the DeeBot land canned responses.  “No worries. Let me assist you further... If you wish to proceed, kindly provide us with the requested info below to proceed.  Let us know if you have any concern.” 

Finally, I told them that it wasn’t working.  I had to shut off DeeBot when she recharged so she wouldn’t start cleaning.  With all this rebooting, she now just sung out at a new time with a “Beep!  You all remember I’m here, right?  And that I can’t clean because you shut me off?”  This leads me to wonder exactly what shutting off means if she can still call out.

The DeeBot company told me I can send her in for repair but that they couldn’t send me a new DeeBot while they did the repair.  “Does this mean I would have to go without my DeeBot while you replace it?  If that’s the case, please never mind.  I can live with this bit of weirdness.  Please confirm.”  For all I know, the new DeeBot might have a worse problem.

Now during dinner every night at 7, DeeBot says, “Beep.  Remember me?”  

Ronnie, being a courteous human, says every night, “Hi, DeeBot.”  We humans see things in personal terms.  I’m pretty sure that is how computers are going to get us.

Currently, I have injured both my shoulders and am awaiting surgery.  With the inability to reach or push, I am unable to vacuum at all.  The good thing is that DeeBot doesn’t need my shoulders to clean the house.  I turn her on and set her loose.  If not for DeeBot, it wouldn’t be pretty at my house.  Dirt and animal hair would rule and we’d just have to throw down grass seed to deal.

“Thanks, DeeBot, but don’t get any autonomous ideas.  I still know where your on off switch is. You can’t live on battery power forever, little missy.  I’m still in charge!”

L’Chaim.

Joceile

1.4.20

[Picture of tan carpeted floor with crisscrossing lines on it.]