The person and parts behind the work

About Durrantula.

My name is Tanner Durrant. I am the maker—and one part of the system—behind Durrantula Wood & Laser in Ogden, Utah.

We make things worth keeping: objects that hold grief, identity, humor, memory, love, and the wonderfully specific ways people move through this existence.

Tanner Durrant smiling outdoors in the mountains, wearing glasses and a lavender shirt

Choose your reading depth

A gentle content note

This story mentions childhood trauma, suicide, self-harm, eating disorders, hospitalization, autistic meltdowns, and dissociation. You are welcome to choose the shorter version, pause, or skip directly to the work.

01

The signs were there

Survival before language.

I grew up in an adverse childhood with an ACE score of 9 out of 10. Long before I had language for autism, ADHD, complex trauma, OCD, eating disorders, or dissociation, my body and mind were already showing the signs.

I learned to monitor the people around me, anticipate reactions, suppress my needs, and keep moving through discomfort. Individuality did not always feel safe. Attention did not always feel safe. Being the version of Tanner other people wanted often felt safer than discovering who Tanner actually was.

One of the most effective tools I found was humor.

If I made the joke about myself first, I could take the punch away from somebody else.

That taught me how to read a room, connect quickly, diffuse tension, market myself, and make painful things approachable. It also taught me to abandon myself before someone else had the opportunity.

I am learning the difference between humor that creates connection and humor that cuts me first. I do not have to humiliate myself to earn safety. Sometimes there is a joke. Sometimes there is a wound. Often, there is room to honor both.

By high school, I was living with depression, suicidal ideation, and self-harm. I also experienced binge-eating disorder and avoidant/restrictive food intake disorder. Food could be comfort, stimulation, predictability, escape, or something my sensory system could not tolerate at all.

I often did not notice hunger, thirst, exhaustion, pain, or the need to use the bathroom until those needs became severe. I could disconnect from my body to complete what was demanded and only later understand the cost.

I did not know that was dissociation. I thought I was inconsistent, weak, dramatic, lazy, or failing. I thought the answer was to push harder.

02

Teen years to early adulthood

Finding ourselves in the shop.

Woodworking entered my life during my teenage years and remained part of it into early adulthood. The shop offered something much of life did not: a process that made sense.

A sharp handplane could take a nearly transparent shaving from a board. A saw could follow a line. A joint either fit or showed you where more work was needed. Rough lumber could slowly become a box, an urn, a keepsake, or something meant to outlive the hands that made it.

Craftsmanship gave different parts of us a place to exist before we understood that we were parts. Some understood tools. Some could visualize how an object should come together. Some could solve mechanical problems, obsess over details, or stay with a process long enough to learn it deeply.

When something became a special interest, I did not dabble. I dove in. That happened with woodworking. Later, it happened with autism. It even happened with grass—because varieties, soil, irrigation, growth habits, and rehabilitation can become an entire universe when an autistic brain decides they matter.

Before “& Laser,” Durrantula was a woodworker. We were a system of skill, craftsmanship, curiosity, and hope in our heart—even before we knew we were a system.

03

Answers that did not quite answer

Diagnosis, misdiagnosis, and missing context.

I was diagnosed with ADHD at 21. Shortly afterward, I was diagnosed with bipolar II disorder. That diagnosis shaped how my experiences were interpreted for years, but it never adequately explained the whole of what was happening.

The depression was real. The distress was real. The shifts were real. The explanation was incomplete.

Autism eventually became a special interest. I read, researched, compared experiences, and looked backward through my entire life. The sensory differences, social performance, intense interests, executive dysfunction, shutdowns, demand avoidance, difficulty recognizing bodily needs, and lifelong exhaustion had always been there.

So had complex post-traumatic stress. So had obsessive-compulsive patterns: the looping search for certainty, the fear that getting something wrong could make me unsafe or harmful, and the urge to analyze an experience until it finally felt resolved. So had dissociation.

These are not tidy boxes in my life. Autism, ADHD, OCD, CPTSD, eating disorders, depression, and dissociation interact. One can disguise another. One can amplify another. A coping strategy can resemble a symptom from a completely different diagnosis when the person evaluating it does not know the full history.

I spent years applying neurotypical advice to a neurodivergent, traumatized, dissociative nervous system. When the advice failed, I assumed I had failed to follow it correctly.

04

Fall and winter 2023

Wood became Wood & Laser.

In the fall and winter of 2023, we began making personalized Christmas ornaments and small edge-lit acrylic night-lights. Adding a laser expanded what we could translate into physical form: names, dates, illustrations, photographs, handwriting, memories, and private jokes.

Durrantula Wood became Durrantula Wood & Laser.

An early personalized wooden Christmas ornament made by Durrantula
One of our early personalized ornaments.
An early edge-lit acrylic cow night-light made by Durrantula
One of our early edge-lit night-lights.

The laser eventually moved to the forefront. It allowed us to keep creating as burnout made traditional woodworking increasingly inaccessible. But “Wood” is not an obsolete word in our name.

There are parts of us who still yearn to return to the shop—to push a handplane, pull a saw, and feel a piece of wood become what we imagined. The laser did not replace the woodworker. It became a bridge when the woodshop became harder to reach.

05

The loss that became data

Grief changed the direction.

In 2023, I lost a dear friend to suicide. I had experienced loss before, but nothing affected me in the same way.

From my perspective now, parts of me had seen—and felt seen by—parts of her that were not seen by the rest of the world. When she died, that connection was severed in a way my system could not simply absorb and move past.

I could have treated the intensity of that grief as another reason to judge myself. Instead, I began learning to treat the disconnect as data.

Not something to shame myself over. Data.

The data said that this relationship had reached parts of me that had rarely felt recognized. It said that my life was not sustainable. It said that I was following in her footsteps unless I made major changes.

To make those changes, I had to turn inward with an open mind—and outward toward a real support system.

One idea I carry from Jamie Marich’s Dissociation Made Simple is that trauma sustained in relationship and community cannot be healed entirely in isolation. When trauma happens in a village, healing also requires a village.

06

Treatment and deeper burnout

When “worse” became more information.

In 2024, after years beneath an incomplete bipolar II diagnosis, I completed my first round of transcranial magnetic stimulation. TMS made a night-and-day difference in the depression.

But treating depression did not make me neurotypical. It did not resolve the trauma, autism, ADHD, OCD, eating disorders, sensory needs, or dissociation. Leaves of absence became part of a repeated attempt to recover enough to resume the same unsustainable life.

In 2025, treatment intensified. Hospitalization, intensive outpatient treatment, ketamine therapy, and a second round of TMS helped treat the depression. As the depressive fog changed, the autistic burnout became harder to miss.

I had turned recovery into another performance—another full-time job with expectations I could fail. Even while healing, I was still going nonstop.

During autistic meltdowns, I have broken my hand three times. I have given myself concussions, caused possible lasting harm, and added self-induced trauma to a body and system already carrying too much.

I do not share that for shock value. Autistic meltdowns are not tantrums or calculated manipulation. They can be the catastrophic overload of a nervous system that has exceeded its capacity. The aftermath does not need more shame. It needs safety, compassion, lower demands, skilled support, and curiosity about what the behavior was communicating.

Every shutdown was data. Every period of disconnection was data. Every treatment that helped one layer while revealing another was data.

The question slowly changed from “What is wrong with me?” to “What is my system trying to tell me?”

Self-recognition, access, and the diagnostic paywall

Understanding myself is not something I have to purchase permission to do.

A professional diagnosis can unlock documentation, accommodations, benefits, or treatment. It can also be expensive, inaccessible, inconsistent, and shaped by whether the evaluator understands masked adults, trauma, neurodivergence, and dissociation.

In my view, pursuing a costly adult autism evaluation simply to obtain permission to name what has been present throughout my life would be futile. A clinician’s report would not create my autism. It would document—or fail to document—the neurotype I already live in.

Why autistic self-identification can be valid

  • Autism begins in development; it does not begin on the day an evaluator recognizes it.
  • Many adults were missed because their traits were masked, punished, misread, or attributed to anxiety, mood, behavior, personality, or trauma.
  • Adult evaluation can require substantial money, travel, time, collateral childhood records, and access to specialists who understand adult presentations.
  • Adult autism tools and services remain imperfect. A negative or inconclusive evaluation does not automatically explain away a lifetime of autistic experience.
  • Using autistic frameworks and accommodations has helped me understand sensory needs, demand avoidance, burnout, communication, and regulation without harming anyone or taking resources away from another autistic person.

Why dissociative self-recognition matters

  • The person living inside a mind has access to patterns, state changes, memory barriers, internal communication, and embodied experiences that cannot always be observed in an appointment.
  • DID is commonly hidden, doubted, and misdiagnosed. Formal recognition may arrive only after years in mental-health systems and multiple prior diagnoses.
  • Naming parts and approaching them with curiosity has given me a safer working model than treating every internal difference as deceit, failure, or instability.
  • A paywall should not determine whether I may use parts-aware language, reduce shame, track symptoms, communicate internally, or ask providers for dissociation-informed care.
  • Self-recognition can be valid without claiming certainty about every clinical differential or refusing competent professional support when it is available.

I live with dissociative identity disorder. For us, that means multiple dissociative parts or self-states sharing one body and one life. Different parts may carry different memories, ages, emotions, needs, abilities, perspectives, or protective roles.

Our parts are not fictional characters. DID is not schizophrenia. It does not make us dishonest, dangerous, or less human. Dissociation was a way our developing mind adapted to experiences that were too overwhelming to hold as one continuous reality.

Recognizing the system did not create it. The signs had been there all along.

This understanding is not happening in isolation or as a rejection of professional care. I am doing this work with the support of a licensed therapist. Together, we can remain curious, observe patterns over time, prioritize safety, and make room for better information without treating a costly formal evaluation as the only place valid self-knowledge can exist.

I also believe in staying open. A self-understanding should illuminate more of life, not require ignoring contradictory information. I can regard my autistic and dissociative self-recognition as valid while welcoming careful, trauma-informed clinical collaboration and revising language when better evidence appears.

What supports autistic self-identification?

The Autistic Self Advocacy Network explicitly includes people who figured out they were autistic on their own and notes that formal diagnosis can be difficult to obtain, especially in adulthood. Research on adult self-identification documents barriers to referral and assessment, while research on adult measures has also questioned how well some instruments correspond with clinical diagnosis.

Read ASAN’s position · Read the adult self-identification review

Why be more precise about DID?

DID is supported as a real trauma-related disorder, and the person’s own report is part of the diagnostic evidence. It is also complex and overlaps with trauma conditions, mood disorders, OCD, neurodivergence, psychosis, neurological conditions, and other forms of dissociation. That makes lived self-recognition important—and careful differential assessment valuable when genuinely knowledgeable care is accessible.

Read the APA overview · Read about epistemic harm and DID

What self-identification does—and does not—mean here

It means I trust the sustained pattern of my lived experience enough to use language that reduces harm, improves communication, and helps me seek appropriate support. It does not mean I am offering a diagnostic method for other people, replacing emergency care, or claiming that every symptom has only one possible explanation.

07

Not separate boxes

The threads in our system.

No single label tells the entire story. These experiences overlap, disguise one another, and change how each is expressed.

Autism + ADHDSensory processing, intense interests, executive function, demand avoidance, communication, masking, and burnout.
CPTSD + dissociationHypervigilance, shame, state-dependent access, disconnection, protective responses, and the compartmentalization that helped us survive.
OCDLoops of doubt and responsibility, the search for impossible certainty, and attempts to think our way into perfect safety.
Eating disordersBinge eating and ARFID as different expressions of regulation, comfort, sensory safety, control, and disconnection from bodily signals.
Depression + griefReal suffering that deserved treatment, but could not explain every underlying need, state, or loss of capacity.
The systemParts with different ages, skills, emotions, beliefs, memories, protective roles, relationships, and access to the body and world.
Tanner smiling in a green mountain landscape
Now we get to learn to love parts of ourselves we did not know existed.

08

A system of makers

Why your stories matter to us.

Before we knew we were a dissociative system, we already spoke about ourselves through Durrantula.

Durrantula was the woodworker. Durrantula was the craftsperson. Durrantula was the collection of skills that could study a tool, solve a problem, and turn an idea into an object.

There are parts who love traditional woodworking. Parts who understand machines. Parts who design. Parts who communicate through humor. Parts who hold grief. Parts who can sit beside another person’s loss. Parts who want to make people laugh with an absurd wallet card, and parts who know why a memorial engraving must be treated with extraordinary care.

We understand that objects carry emotional weight because memory, identity, grief, and connection are not abstract ideas in our life.

A memorial can give grief somewhere to land. An anniversary gift can hold years of private history. An engagement piece can mark the beginning of a shared future. An identity-affirming object can say, “I see who you really are.” A sarcastic wallet card can transform shame into humor—or simply become the exact ridiculous object someone did not know they needed.

When someone brings us a photograph, name, loss, inside joke, identity, celebration, or “okay, hear me out” idea, they are trusting us with a small piece of their humanity.

We do not take that lightly.

09

How we are changing

Compassion can take us where shame never could.

For years, I survived by getting ahead of the joke, suppressing the need, disconnecting from the body, performing competence, and pushing through.

Those strategies deserve compassion. They helped me survive circumstances in which being fully visible did not always feel safe. But survival strategies are not sacred obligations.

I am learning that humor can connect without cutting me first. That a need is not a moral failure. That capacity is not character. That a meltdown requires care, not punishment. That grief can be information without becoming a sentence. That dissociation is not proof that I am irreparably broken.

I am learning that every part of us formed for a reason—and that our worth has never depended on how convincingly we could perform being okay.

We are not at the end of this story. We are still recovering from burnout. We are still learning our system. We are still grieving. We are still discovering what kind of life allows all of us to exist safely.

Durrantula Wood & Laser is one part of that becoming. It is where survival meets craftsmanship. Where grief meets remembrance. Where humor meets truth. Where an idea becomes an object—and an object becomes part of someone’s story.

Whatever brought you here, thank you for allowing us to become a small part of your journey through this existence. It is an honor.

Support and disclosures

You do not have to carry a crisis alone.

This page contains one person and one system’s lived experience. It is not therapy, diagnosis, crisis counseling, or medical advice. Reading it may bring things up. You are allowed to stop and reach for support.

988 Suicide & Crisis Lifeline

Free, confidential support in the United States, 24 hours a day. You can reach out for suicidal crisis, emotional distress, or concern about someone else.

Utah crisis support

Utah’s 988 service connects people with trained crisis workers and can help determine whether local mobile crisis support or another safe next step is appropriate.

Utah 988 resources

Weber Human Services

Local behavioral-health services at 237 26th Street in Ogden. Their published intake number is 801-625-3700.

Therapy and diagnostic disclosure: Tanner is exploring these experiences with the support of a licensed therapist. This account reflects lived experience, extensive self-study, treatment, and ongoing therapeutic work; it is not offered as a template for diagnosing someone else or as a rejection of professional care. Self-identification can be a legitimate tool for self-understanding and accommodation, while trauma- and dissociation-informed clinical collaboration can support safety planning, differential understanding, documentation, and treatment. If there is immediate danger or a medical emergency, use emergency services rather than relying on this page.

Immediate support

You are allowed to reach out before it becomes unbearable.

The 988 Suicide & Crisis Lifeline offers free, confidential support in the United States 24/7 for suicidal crisis or emotional distress.

A pause is allowed

You do not have to finish this story right now.

Notice where you are. Let your eyes find something familiar. Set the page down, get a drink, contact someone safe, or return when you have more capacity. Nothing here requires you to push through.