psychology

Father’s Day

Posted on by SomatiCat

Probably fortunately, I only ever had one father—so I assumed all fathers were like mine. I didn’t understand why Father’s Day was such a big deal.

He passed away long ago at the ripe age of 87. From the outside, he looked like a “good enough” father. He provided for us and supported my brother and me through much higher education than he ever had. And yet—I hated him. As far as I know, my younger brother felt the same.

He never hit us. But he was emotionally and verbally abusive, especially toward my mother and me. When I visited my parents, I stopped talking to him. My brother wouldn’t even set foot in the house. Later, when Alzheimer’s took hold, he was admitted to a nursing home. I didn’t love him, but as a “good enough” daughter, I visited him every day while I was in town. He didn’t recognize me. I sat beside him, spoke gently, massaged his shoulders. He wasn’t as nasty as before—maybe because he no longer knew I was his daughter. Still, from time to time, he shouted cruel things at the other residents. The staff would smile and say, “That’s the dementia talking, not him.”

But I turned to my mom and said, “That’s exactly how he always was.”

Since childhood, I’d been the main target of his emotional outbursts. In a nutshell, having a daughter was, to him, a waste. He made it clear he wished I hadn’t been born a girl. He told me I was too ugly to be loved by anyone. That became the foundation of my identity.

I grew up believing I wasn’t lovable as I was. That I would never be good enough for anyone. I didn’t trust men. I hated him.

Still, I did what I could out of duty. He died alone. I made it to his wake and funeral. No one cried.

I have a friend I’ve known for 30 years. Her worldview is completely different. She loves her parents deeply, and they love her. Her father lives in assisted living and is adored by the staff. He always told his three daughters they were cute and pretty, just as they were. Being his daughter was reason enough to be loved. Her older sister treats her own daughters and granddaughters the same way. My friend says love flows naturally in her family. She believes in love. She knows she is beautiful, and she knows she deserves love from men.

I once told her, “I don’t understand love.” She didn’t understand what I meant—until we shared our stories.

Not all fathers are the same. Not all families are the same. Not everyone’s idea of love is the same.

I can understand, at least partly, what made my father the way he was. I can feel compassion for him. But I still don’t love him. I never felt loved by him. That kind of feeling, I reserve only for my dogs.

So on Father’s Day, while many people celebrate, please remember:
Some of us can’t.

Multiverse Madness

Posted on by SomatiCat

You may have heard the famous Eastern philosophical parable about a man who dreams he is a butterfly, only to awaken and wonder: is he a man who dreamed he was a butterfly, or a butterfly now dreaming he is a man?

Doctor Strange in the Multiverse of Madness reminded me of that parable. In the film, dreams are portrayed as stories unfolding in alternate universes. Interestingly, the only person who can travel through the multiverse is the one who has never dreamed.

Have you ever had the same dream over and over? Not exactly the same, but different variations on a single theme? I used to have dreams like that.

One of the recurring dreams I had after a messy divorce was about my ex-husband. In those dreams, he had remarried and had a daughter and a son. They were some of my worst nightmares. He had cheated on me while I was undergoing infertility treatment, and by the time we divorced, I was too old to conceive. I had lost my chance to become a mother.

I dreamed this scenario again and again. The emotional anguish felt so real, it lingered even after I woke up. His betrayal stained the landscape of my inner world with grief and suffering. In waking life, I felt mostly anger—but underneath it, I carried a deep well of loss and sorrow.

In these dreams, I always lived in some kind of apartment. Each one felt strangely familiar. Sometimes I would find myself in the exact same apartment I had dreamed of before—with the same landscaping outside, the same scent in the air, the same humidity in the walls. I knew that place.

It’s been twenty-five years since the divorce, and I’ve finally stopped having that dream. Still, it feels as if I once lived in that apartment—in this life.

Then I began to wonder: maybe that was my life in an alternate universe. It’s about the inner choices we make—who we decide to become. Every decision spins off another timeline, another universe where a different version of you lives out the consequences of that choice.

If I had clung to the anger and suffering, maybe that nightmare would have been my reality.

These days, I rarely dream. Maybe my life has finally settled into this reality.

P.S. My ex-husband did remarry, but he never had kids. As for me, I’ve made peace with the fact that motherhood and I were probably never meant to be. Crisis averted—for the children.

Ding Dong, the Witch is Dead

Posted on by SomatiCat

I got a call from my 92-year-old mother. She had just been informed by the nursing home that my 100-year-old aunt passed away in her sleep—her heart had stopped.

I had visited her just a month ago and sat with her, talking. She had stopped responding a long time ago, but her heart kept beating with the help of a pacemaker. She swallowed whatever mushy food her caregiver spooned into her mouth and wore diapers.

This is not how I want to spend the last years of my life.

I loved her when I was a child. She lived next door to my parents, and she spoiled me with sweets, cute dresses, dolls, and stuffed animals—whatever I wanted, she bought for me. Every day, I waited eagerly for her to come home and ran to give her a hug. Sometimes, her breath smelled of alcohol.

My father was emotionally abusive, and my mother was emotionally unavailable. In many ways, it was my single, childless, career-oriented aunt who “adopted” me. She even wanted to adopt me legally at one point, but my parents—outraged—refused. There was no reason for them to give me up; we weren’t poor. I suppose it was her desire to have a daughter of her own.

I used to say I wanted to be just like her. She was my role model: fashionable, independent, capable of doing anything perfectly. She was the first woman in the region to be promoted to regional manager at the national telephone company. She was also incredibly skilled with her hands—especially knitting and crocheting. I had so many beautiful sweaters she made, and people often complimented them.

I, on the other hand, am not crafty at all. I tried, but I could never do anything as well as she could. I’d get frustrated, give up, and she would finish my projects for me. I still sometimes try, but I almost always give up.

She kept her home neat and beautiful, always with fresh flowers from her garden. She adorned the house with lovely things. Though she didn’t cook elaborate meals, she arranged simple dishes with such care that they looked more appealing than my mother’s “here’s your food, eat” style.

I admired her and, as a little girl, I dreamed of being like her—working, unmarried, and childless. That was an unusual dream at the time, when most girls wanted to be brides in white gowns. My parents didn’t respond to my dream at all. They just ignored it.

Life didn’t turn out quite the way I envisioned. I moved to the U.S., got married, worked as an ordinary office assistant, got divorced, lost my job, became an independent contractor, and remained childless. Still, I returned to Japan once a year to visit my parents and my aunt.

Even as a child, I sensed something was off in my family. There was a ghost in the closet—a family secret. Children can feel these things. Even if it’s never spoken, it changes the air.

The closet opened after my father—my aunt’s younger brother—passed away at age 87. My mother began to talk.

It was the scandal everyone in the small town knew. My aunt had an affair with her married boss and got pregnant. At the time, having a child out of wedlock was a deep shame for a respectable family. But she refused to have an abortion. Her lover’s wife was infertile, and my aunt may have believed that having a child would lead him to divorce and marry her.

Instead, he and his wife adopted the baby girl. He secretly allowed my aunt to visit the child, pretending she was just a family friend. But my aunt, lacking boundaries, acted like a mother. As the child grew older and started asking questions, the visits ended. The wife eventually died, but the man never remarried. The girl grew up not knowing she was adopted until her teenage years.

Then I was born into the family. At the time, my parents lived with my grandmother and my aunt. In a sense, my grandmother gave me to my aunt as a substitute. I don’t remember my mother’s touch. I was always with my aunt. Four years later, my brother was born, and this time my mother clung tightly to him. He was always wrapped around her like a baby monkey.

Once the secret came out, the meaning of so many things shifted. When I used to say I wanted to be like my aunt, I meant I wanted to be an independent woman. But my parents may have heard something else—that I admired her for having an affair and bearing a child out of wedlock, bringing shame to the family. My father resented having a daughter—specifically me being a daughter. From him, I absorbed the belief that all men were predators, and I had to fend them off with claws and fangs.

My aunt loved me like a daughter until she lost her mind. Even in my fifties, she’d try to brush my hair and spoon-feed me. She never truly saw me for who I was—only the daughter she lost. I was her living doll.

After my father died, my aunt’s physical and mental health declined. No one in the family wanted to take care of her, and I was the only one who didn’t hate her. So, by default, I became the one responsible.

She lived in her own home for nearly ten years, with various caregivers as her condition worsened. Eventually, she needed 24-hour care.

That’s when her true nature came out. She was highly narcissistic and very demanding. She wanted everyone around her to serve her in exactly the way she expected. She went through so many caregivers. She never forgot who had crossed her.

“Everyone who spoke ill of me died of cancer,” she once said, as if she’d cursed them.

Yes, she cursed me with her projection. She cast me in a role she needed someone to play—and I played it well. I understand she had a hard life, and she endured it the only way she knew how: by casting her pain outward, cursing everyone around her.

After the phone call, I said to myself, “Ding dong, the witch is dead.”

At least I’ve chosen not to curse anyone. That is my freedom.

Do I want to see tomorrow?

Posted on by SomatiCat

I lost my anchor.

My dog was my tether to reality, to this life. He was undeniably real. He lived entirely in the moment. When I woke in the middle of the night, lost in the vast nothingness—confusion and darkness pressing in—I would reach out and place my hand on him. He was warm, solid, breathing. Alive. And in his version of reality, if he was alive, then so was I. I felt safe in the world he held for me. It was as if I were drifting in a night ocean of existential anxiety, and he was my life raft.

With his passing, I lost my favorite version of reality.

I don’t have to protect anyone. I don’t have to take care of anyone. I don’t have anyone to come home to. I don’t have to worry about losing him anymore.

What remains is my own version of reality.

Every morning, I wake up and start my routine. I make coffee, brush my teeth, check emails. I function well. I smile. I chat with neighbors. I act normal. But I am not here. I’m floating an inch above the ground, like a plastic bag caught in the wind, weightless and directionless.

Once in a while, I do feel real. On a recent trip, I went to a shooting range and practiced pistol shooting for the first time. In that moment, I was completely focused. The weight of the gun in my hands, the shock waves reverberating through my body, the hot shells grazing my skin—burning, tangible—I felt alive. For that brief moment, the act of shooting was my anchor. (Don’t worry, I won’t shoot any living being, including myself.)

Then I came home, and my fragmented reality returned.

Fortunately, I can hold it together. I don’t have the affliction my cousin does—the one that warps reality beyond repair. I can pretend. I can fit in. I just don’t feel alive.

So I go to the gym. I work out on one of those torture machines. The intense contraction in my quads pulls me back into my body, back into the present.

Do I want to see tomorrow?

I don’t know.

But I want to be here now. In my body.

Is it how normal people are feeling?

Posted on by SomatiCat

I sent my beloved dog across the rainbow bridge one month ago, and I’ve been depressed ever since. I still cry and feel his absence deeply. The sharp pain and heaviness in my chest have lessened, but they’re still there.

I go out every day—talking to neighbors, having lunch with friends, attending events I’m invited to, and spending hours at the gym. I’ve been working out daily.

Without the need to walk my 80+ pound dog three times a day, I suddenly have more uninterrupted time. I’ve been channeling that into my writing project, which is progressing well.

I also have two trips planned, something that would’ve been impossible when I was caring for a 13-year-old large dog. I’m doing everything I can to avoid spending days in bed, mindlessly watching Netflix all day and night. I’ve been there before. I know how it happens, and I know how to prevent it.

At the same time, multiple changes have happened in my life—not particularly happy ones.

From the outside, I probably look fine. I’m functioning well. But I’m not okay. I don’t feel alive.

Even when I laugh, enjoy conversations with friends, or run on a treadmill for an hour, I feel… hollow. Like a cow, grazing mindlessly on grass, waiting to be slaughtered, unaware of its fate.

And I ask myself: Am I depressed? Or is this just how most people feel, going through the motions of everyday life?

On Facebook, everyone presents their happy, vibrant lives. But are they really alive, or do they just think they are?

As the old Chinese parable says: Am I a monk dreaming of being a butterfly, or a butterfly dreaming of being a monk?

Touch: Your Brain’s Interpretation

Posted on by SomatiCat

Even though the sensory receptors in the skin are mechanoreceptors, it is your brain that interprets the signals they send. Since the brain remembers past experiences and the emotions associated with them, touch is never merely a  touch. Even the same mechanical touch can be felt differently—it can be loving, caring, comforting, or healing; sensual or sexual; cold, abusive or invasive. Even when you think your touch is neutral, it’s up to the receiver’s brain to interpret it.

When I was in my late thirties, I went through infertility treatment. To check if my fallopian tubes were open, I underwent a very uncomfortable test. The pressure I felt inside my body was so invasive that I instinctively contracted my entire body, bracing myself. Then the technician’s assistant gently placed her hand on my arm. I melted. Her touch was neutral, and I don’t think she was consciously trying to comfort me. I felt it came from her spontaneous empathy. 

I have Meniere’s disease. One day, I had a Meniere’s attack in a gross anatomy lab and had to lie on a cold linoleum floor for some time, clutching a barf bag. I told everybody that nothing could be done to relieve my suffering and asked them to keep me safe and leave me alone until the symptoms resolved. I threw up in the bag and was hyperventilating in a fetal position. Some people can’t tolerate witnessing suffering without doing anything; it might make them feel powerless. A few of them placed their hands on me, perhaps to soothe or heal. I just had to endure the unwanted touch. They were mechanically the same kind of touch, but my brain interpreted them differently. One was comforting and the other was annoying.

As a child, I experienced improper touches, which were a violation of boundaries. This experience made me sensitive to the intent behind a touch. I don’t remember receiving loving touches from adults in my family during my childhood. My nervous system used to react to every touch as if it were a danger. Sometimes, a touch triggered tremendous rage, while other times, it made me feel nauseous. It took me a long time to learn to discern a safe touch from an unwanted one. I’ve learned to set boundaries and to choose how to respond, not just to react. 

copyright 2024

Why Me?

Posted on by SomatiCat

When you get hit with incurable, degenerative, and progressive diseases, you would probably say, “Why me?”. The life you believed you would have ends with the diagnosis. The person you have been dies with the diagnosis. You don’t know what you could expect for the future, except for the fact you would lose everything you thought you would have.

Why me? We don’t have any answer to that question. My friend, Maria, was diagnosed with ALS and passed away within a year. Every day she lost some of her function. She said that somebody told her that the Universe/God had chosen her because she was strong enough to handle it. “I didn’t want to be chosen for this,” she said. It was the most cruel answer to the question.

I have a friend who was diagnosed with Parkinson’s disease. Once an epitome of fitness, he had worked in the fitness industry for the entire life, training diligently. He is losing his physical function. He didn’t do anything wrong to deserve it. “Why me?” he must have asked.

I have a friend with scleroderma. Her physical movements are limited and is constantly fighting against its progression. Mundane issues of life, such as dentistry treatment, become huge challenges. She must have asked, “Why me?”

All of them are strong and facing the challenges. They are wonderful people. Why them? There are no answers.

If you don’t have any of these disease, you would never think, “Why not me?”

When I was hit with Meniere’s Disease, I cried out, “Why me?” Meniere’s Disease is incurable and degenerative. It is rather unpredictable than progressive. I couldn’t leave home without the fear of severe attacks, which would render me incapacitated. I lost the life I expected to have, bedridden most of days. I am tenacious by nature, so I fought to regain my function with teeth and claws. Did I do anything to deserve it? Actually I did. Eventually I figured out the trigger. It was my genetics and lifestyle that triggered it. Even though Meniere’s Disease is incurable, I am managing it with very strict lifestyle change and am currently in remission.

Now when I think about my friends with ALS, Parkinson’s, Scleroderma and other incurable, degenerative, progressive diseases, I think, “Why not me?”

I am dodging the bullet every day, every moment, as they are stealing every single day from the illness.

So, if you don’t have these illness, you are blessed. Be grateful and savor every moment of your life. You are probably dodging bullets without knowing it.

Skin

Posted on by SomatiCat

Where body meets air we are all cadavers

The Body: A guide for Occupants by Bill Bryson

Epidermis

Epidermis

I walked into the gross anatomy lab at a medical school, wearing a brand-new white lab coat, and stood at one of the dissection tables. The steady hum of  the air purifier filled the room. Under the gleaming florescent lights, the lab appeared sterile and lifeless. It held multiple tables, each with a cadaver lying upon it. It was my first human dissection class, and I was nervous. Unless you are a medical student, funeral director, coroner, forensic examiner, or some kind of specialist, you rarely have the chance to see naked dead bodies quietly resting on stainless steel tables. The cadavers were embalmed for preservation, giving their skin somewhat foreign texture.

In my old country, we don’t have the custom of embalming. When my grandmother passed away, she was laid on a futon in her home, as if she were sleeping, and family members took turns staying beside her body through the night. It is an old tradition for family members to spend the last night with a loved one—a way to familiarize the living with death. I stayed with her body for several hours, keeping incense burning. Her skin was yellowish, wrinkled, and dry but otherwise intact. The cold air from the dry ice, used to slow the body’s decomposition, seeped through the futon, carrying with a faint, distinct whiff of death.

In the lab, the cadavers’ skin was unnaturally moist due to the embalming fluid saturating their tissue. We carefully observed the artifacts of death and embalming process to distinguish them from the inherent characteristics of the deceased. The outer layer of skin was peeling in patches, similar to sunburned skin but slightly deeper. This is a decomposition process where the bond between dermis and epidermis begins to break down. One of the cadavers was a dark-skinned man, and we were startled to see the pale skin layer beneath. We realized the skin color is only epidermis deep. Beneath the epidermis layer, we are all same color: pale and fair.

The epidermis, the outermost layer of skin, is only 0.05mm (on the eyelids) to 1.5mm (on the palm and sole) in thickness. It defines our social identity, being the first aspect others notice. It is a social organ. As a person of east Asian origin, my skin has an olive tint.  When I was a child, I spent most of my time outdoors and became tanned in the areas exposed to the sun.  Naturally I was darker than adults who spent most of their time indoors. My father used to tell me I was too dark to be considered pretty. In my old country, at least at that time, fair skin was idealized as a standard of beauty for women; the lighter, the better.  My skin is still tanned, though not as much as when I was younger. In fact, the parts of my body that rarely see sunlight are as fair as those of my friends with natural light skin. I simply don’t burn as easily as they do. Being labeled as an “Asian girl too dark to be pretty” haunted my self-image, even though it was just an epidermis-deep judgement, easily shed like a snake’s slough when it no longer fits. Today, I am a proud woman of a certain advanced age with beautifully tanned skin, less sun-damaged than that of some fair-skinned friends.

Melanocytes, located in the bottom layer of epidermis, produce melanin, which determines skin color. Without the epidermis, you would be pale. Defining people by skin color is absurd. Melanin protects the skin from UV damages caused by sunlight. A darker skin color simply means your skin is more tolerant to UV exposure. 

In the living body, the deepest layer of the epidermis, where melanocytes reside, is firmly attached to the dermis and does not peel away easily. Since the epidermis lacks sensory nerve endings — except for vibration-sensing Merkel cells, which are found in the bottom layer— touching the epidermis itself does not produce sensations. However, there is a rare genetic disorder in which the bond between the dermis and epidermis is very weak, causing the epidermis to peel away with the slightest contact, exposing nerve endings. Individual with this condition are vulnerable to UV damage, infections, and other external threats. Imagine being without an epidermis. Every slightest touch would cause excruciating pain, and your existence would become a constant agony. When I studied psychology in a post-graduate psycho-spiritual counseling program, the instructor described a person with borderline personality disorder as “being without skin.”  The analogy might be more accurately described as a condition of being without an epidermis.

The epidermis forms the boundary between what is me and what is not me, serving as the first line of defense by protecting what is inside from the external environment. Despite its crucial role, it is less than 1mm thick. Our physical existence is remarkably vulnerable in this way.

When I get a temporary henna tattoo, the “tattoo” fades away in a week or two because the pigment only penetrates the epidermis.  The outermost layer of the epidermis, the stratum corneum, consists of dead cells that are constantly flaking away. The cells in the outer layer of epidermis are replaced every thirty to forty days. Part of us is constantly dying from birth. Our physical existence is not as separate as we might believe. When I step into a subway car, I sometimes encounter a distinct smell associated with a particular human state. Even if the source is no longer present, the oder lingers as if the ghost of its presence remains. Occasionally, we find ourselves in someone else’s personal space, and as I inadvertently breathe in tiny molecules of oder, I also realize I am inhaling minuscule flakes of dead epidermis. 

As a manual therapist, when I touch a client, I make contact with their epidermis. I would never touch their dermis, the true skin, directly. Between “them” and “me,” the epidermis stands guard, keeping “not me” out.  Every caress of lovers passes through the layer of dead cells. Flaked-off dead cells mingle with other minute substances, floating away in the air or settling on the floor. This thin, evanescent boundary keeps us safe from one another.

The first difference between a living person and a cadaver lies in the skin. In the dissection lab, we stood around a table with a cadaver. No one touched it until the instructor encouraged us to do so. Initially, most of us hesitated, but soon we began to touch the cadaver quite aggressively. The cadaver allowed us to explore in whatever way necessary for study. A person has boundaries; a cadaver does not. When somebody violates your boundaries through inappropriate touching, they are treating you as if you were a cadaver.

Imagine yourself as a corpse lying on the ground. Focus on the outermost layer of your skin. Peeling away in patches, this interface with society falls off. It becomes desiccated and papery—light and fragile. Part of your identity sheds away, your boundary dissipating with a mere whiff.

copyright 2024

Meditation on Cadavers-Prologue

Posted on by SomatiCat

Savasana

I am not writing an anatomy book, nor a dissection manual, though I use nomencIature of anatomist when it is more clear than everyday language. This book/writing is not about scientific knowledge. If you want to learn detailed anatomical information, there are tons of great books you can choose from. This is just A story of my personal experience facing cadavers in dissection labs, and a story about how that experience has affected my perception of who I am, how I relate to everything, especially to my body, in this lifetime.

I once read about a meditation technique where you lie on your back and imagine your body gradually decomposing until it becomes a skeleton. I heard that in Buddhism there is a meditation method in which one observes one’s own body both from the inside and outside while observing an actual corpse decompose. I liked this meditation method because I interpreted it as a training to realize that all material existence in this world, including one’s own body, is a mere phenomenon, just like a decaying corpse. 

When we experience unbearable trauma, our body and consciousness may become dissociated in order to protect ourselves. The body becomes a thing that performs a specific function, and becomes separated from the ”I” consciousness.

Once I had sessions with a Zen psychology therapist. He often asked me, “What do you feel in your body?” I looked up at the ceiling, looked around the room and always looked for the answer outside of my body. “Can you feel your feet on the floor?” he asked. Of course I could feel my feet physically touching the floor, but that was completely disconnected from what I was feeling mentally. 

I didn’t have much knowledge about my own body. So even when I meditated on a corpse, I couldn’t visualize it very well, and I had no conscious connection to my body, so the corpse quickly turned into abstract bones. I couldn’t understand how complex and delicate the human body was, and how it was related to my very existence.

Through the gross anatomy training, I gradually recovered the connection between my self and my body. Every time I stood at the dissection table, I felt like I was slowly regaining my humanity. It has been more than 10 years since I was initiated into human dissection, and I have spent over 1,500 hours in dissection labs. Now attending an annual dissection workshop is like a Zen practitioner regularly practicing at a temple. 

I see it as my spiritual practice. It prepares me for the reality of death and dying, and reminds me of the meaning of living this moment. 

Savasana in yoga is said to be a pose where you lie on your back and imitate a dead body. When we go to a dissection table in a dissection lab, we face a donated body that is quietly in Savasana pose. It is the last pose we all will take.

copyright 2024

Split

Posted on by SomatiCat

I watched Split and Glass on Netflix, where a fictional character with Dissociative Identity Disorder (DID) develops a personality with superhuman strength. James McAvoy was phenomenal, shifting seamlessly from one persona to another on screen. The story is a textbook case of severe childhood trauma: the psyche fractures to protect the vulnerable self. One of his identities, “The Beast,” punishes the undamaged—those who haven’t suffered.
[Spoiler Alert] The Beast sees the damaged as pure.

That’s what drew me in.

I have a friend with DID. Sarah is brilliant, cultured, well-read, and funny. She took many younger, “damaged” women under her wing. She was the one who introduced me to Broadway, gifting me tickets to Sondheim. We’d sit in cafes, visit restaurants, and talk about arthouse films and everything else. Her life sounded like a novel. She told me she was one of the first female TV producers—or something close. I’m not sure if Sarah is the original. I met two of her other selves: Tommy, a boy who constantly said, “Sorry,” and another, terrifying one—probably her internalized mother.

The switches weren’t as clean as in the movies. She once said she had a “Flat Earth Committee” in her head, which decided what she could or couldn’t do. That committee often said she wasn’t allowed to leave her apartment.

Before her DID diagnosis, she’d been given a charcuterie board of mental health labels: agoraphobia, depression, anxiety disorder. She’d been prescribed all kinds of medications. None of them helped.

Many friends tried to help her. After all, when she showed up as “Sarah,” she was wonderful. But over time, that became rarer.

I was the last one who tried hard. I had this urge to rescue someone else—maybe instead of rescuing myself. Her disorders were inflated versions of mine, so I could speak her language to a certain extent.

I don’t have DID. I’ve been dissociated, but not to that degree. I had dysthymia and episodes of major depression. Sometimes I wasn’t “allowed” to get out of bed. I had extremely low self-esteem and poor communication skills—unless I was in a professional setting. Then I became articulate, competent, impressive. I still have a voice inside that occasionally whispers, “Jump” or “Kill yourself.”

Over time, I realized that some of Sarah’s other personalities were sabotaging anything that might make her better. Whenever she admitted to feeling improvement, they lashed back—as if healing would erase them. As if their survival depended on her staying damaged. Ironically, their original role had been to protect her.

They exhausted me, as they had exhausted many before me.

I haven’t seen Sarah in years. She reaches out once in a blue moon—only in moments of desperation. The last time, it wasn’t even her. A mutual friend contacted me because no one had heard from her. Turned out she’d fallen and been hospitalized. She didn’t have her phone in the hospital room, so she couldn’t reach anyone. But she came up with an ingenious solution: she befriended the woman in the next bed and asked her husband to deliver a handwritten note to my building.

That’s Sarah—resourceful and fiercely capable when it matters. She once told me she’d made a deal with the “committee” to keep her alive. One of her friends with DID had died by suicide. Sarah wasn’t going to be one of them.

Eventually, I accepted Sarah as she is. There’s no “original” Sarah waiting to be recovered. She was already many when I met her. I just didn’t know it. She contains multitudes. Every piece of her is my friend. And I’ve let go of the childish fantasy that I could save her—or anyone else.

Everyone splits, to some degree.

There are incidents I don’t remember, but my body seems to. I don’t have a single, monstrous trauma, just layers: a verbally and emotionally—possibly sexually—abusive father; a manipulative, passive-aggressive mother; a narcissistic aunt; a silent, possibly borderline grandmother. Add to that a culture soaked in misogyny, inappropriate touches, and the absence of loving contact—and I was left scarred.

I didn’t split, but I did build personas: a tough bitch and an abrasive man—my internalized father—to protect the vulnerable child inside me.

I’ve spent decades re-parenting that little girl. I wanted her to grow up into who she could have been if she had been loved and left alone: a happy, loving, beautiful girl. A confident, capable woman who could love and be loved.

I didn’t become exactly what I hoped—but I like who I’ve become. I’m happy with this version of myself.

You can’t restore the original child. But you can hold your scars with tenderness. You can carry your pain gently, like something sacred. And in doing so, you become who you were always meant to be:

Clean and pure, with old scars.
Survive. Then thrive.