Showing posts with label women's mental health. Show all posts
Showing posts with label women's mental health. Show all posts

Thursday, May 14, 2026

When the Light Fades: Let's Talk About Depression and Its Role in Bipolar Disorder - Part 2

When the Light Fades: Let's Talk About Depression and Its Role in Bipolar Disorder - Part 2 of 5

The Heavy Quiet, When the Light Fades

Depression is not just sadness. It can feel like emotional dimming, identity loss, and disconnection from self, especially when experienced with Bipolar disorder.

When I am experiencing “low mood,” I feel completely numb to the world around me. My low moods are sudden, and the physical side effects are apparent. My energy feels completely drained, like a battery that has suddenly used its last drop of power and become a solid mass with nothing left to offer. Though it still looks like a battery, it may even appear as if the battery still has power, but it does not. It is essentially empty.

That is how I describe what depression does to my body and mind. It leaves me like a battery with no power. I appear to be myself, however upon closer examination, the first characteristic people say is missing is my “ever-present energy.”

I can remember the first morning I felt like a drained battery. I was 16-years-old, and my grandmother came into my room one morning, as she did every morning, to wake me up for school. She called out to me once, twice, three times, and although I could hear her calling, I simply could not move. I could not even respond to her in any coherent way.

After she walked out of my room to wake my little sister, I tried to move and couldn’t. I became fearful that something was seriously wrong, and it was. I did not have the energy to speak, and I felt extremely tired. Shortly after, my mind and body succumbed to exhaustion, and I fell asleep.

When I woke up, I was disoriented and still tired. My room was pitch black, and outside was covered in darkness. The trees were cloaked in shadows, and the only gleam breaking through the night came from the streetlights. I stared at those lights, wondering how I could have slept that long and why I still felt drained of all energy. I stared out my window at the glow of the streetlight until even that light faded into darkness, into sleep, into oblivion.

For some, depression comes swiftly, like a sudden shift. For others, it is a slower onset brought on by any number of factors. In my experience, depression can come on very quickly depending on the negative situation, such as death, job loss, post-hospitalization, medication changes, or even the time change during Daylight Saving Time.

It feels like one day I am functioning at my baseline energy level, then I go to sleep and wake up the next day unable to get out of bed. Externally, I may appear calm, but I am unable to show the fear and anxiety that would normally have my body trembling, or cry the tears of frustration my mind wants to release. Instead, there is a complete absence of emotional expression on my face and an internal heaviness that nauseates my stomach.

Depression does not always arrive loudly. Sometimes, it settles quietly and deeply.

This blog focuses on my lived experience with depressive episodes within Bipolar disorder. I will attempt to help you understand what depressive states feel like, how Bipolar depression can feel distinct from general sadness, and the emotional weight, identity shift, and internal silence that can come with it.

What Is Depression, Really?

Unlike sadness, which is usually situational and passes, depression begins for me when sadness does not pass. When sadness becomes a persistent low mood and emotional disconnection, I know I am starting to feel depressed.

When my grandmother passed away in 2004, I shifted from sadness into debilitating emotional pain that crippled me. I was unable to get out of bed. I started using substances to numb the pain, which quickly became part of my depressive journey. I was not simply lacking motivation for activities of daily living. I stopped caring.

I did not care that I was in my fourth year of university, my toughest year, or that I had thesis papers overdue. I did not care about hygiene practices like brushing my teeth, doing my hair, or taking a shower. The only thought I was fixated on was that my grandmother was gone, and she was never coming back.

I stayed in bed for days and weeks at a time, not eating, not really sleeping, but simply immobilized, staring at a fixed object, the floor, or the ceiling, thinking about her.

Grief can be a powerful catalyst for depression.

According to the Diagnostic and Statistical Manual of Mental Disorders, also known as the DSM-5, there are several types of depressive disorders, including:

 Persistent Depressive Disorder
Bipolar Disorder with symptoms of depression
Major Depressive Disorder
Seasonal Affective Disorder
Postpartum Depression
Psychotic Depression
Situational Depression
Treatment-Resistant Depression

Over the years, I have struggled with four of the above: Treatment-Resistant Depression, Situational Depression, Seasonal Affective Disorder, and Bipolar disorder with symptoms of depression. For each condition, depression presented itself differently.

With Treatment-Resistant Depression, which I experienced early in my mental health journey, I had night terrors, sweats, trouble staying asleep, and dangerous thoughts related to my own life. My psychiatrist at the time tried several different antidepressants with similar results and recognized that the depressive symptoms I experienced as a result of Bipolar disorder could not be treated with standard depression medication alone.

With Situational Depression caused by experiences like job loss or the end of a romantic relationship, I found that although I experienced depressive symptoms such as sleep disturbance and low energy, my moods would shift from day to day or week to week. Often, visits from friends, a good conversation with my mom, or support from another relative was enough to lift my spirits and give me hope that the depression would eventually come to its natural conclusion.

The depression that comes with Seasonal Affective Disorder has always been the most challenging for me because of how long it lasts. When Daylight Saving Time ends on the first Sunday in November, I can feel depression creeping into my system two to three weeks before. I become extremely tired as it gets darker earlier. I lose motivation for activities of daily living, and like an animal in hibernation, I sleep for most of the day, only getting up to use the bathroom or get something to eat.

My energy for tasks like writing or exercise becomes almost non-existent. This lethargy typically lasts throughout the winter until Daylight Saving Time begins on the second Sunday in March. There are pockets of energy during this time that allow me to perform simple tasks like cleaning my house, practicing good hygiene, going to church, or visiting my parents. However, these bursts of energy are few and far between.

Bipolar Depression: A Different Kind of Low

Bipolar disorder includes both high moods and low moods, each characterized by a unique set of symptoms. With Bipolar depression, those who experience it can feel emotionally flattened or disconnected from the world around them, especially from the people who want to help them in their recovery journey.

During these depressive episodes, it can be difficult to explain your internal emotional state. Often, the only words that come close are “empty,” “drained,” or “nothing.”

Bipolar depression is far different from general sadness because it can feel like there is no clear beginning or end point. One minute you are living, breathing, and part of the world around you, and then suddenly the world goes black, blurred, and empty. The space your world used to fill becomes hollow. You are empty.

You have no idea why it happened, how it happened, when it will go away, or even how you feel about being enveloped in nothingness. All you can do is wait until it passes and hope you make it through another depressive episode.

The depressive symptoms I experience as a result of Bipolar disorder feel like what I have just described. These symptoms come in cycles, usually lasting two to three weeks before my mind shifts back toward mania or psychosis.

Naturally, my baseline leans toward hypomania: high energy, high productivity. But when I am experiencing depression during a Bipolar episode, I become very still, and my mind cannot hold onto a thought. It feels like a brain drain. Where thoughts are supposed to live, there is only emptiness.

My limbs feel heavy, my body feels hollow, and I am unable to find my voice or speech. This depression is what I consider my most dangerous state because I am unable to communicate clearly with those around me about how they can support me.

This lack of connection can be the most difficult part of the episode. When you experience Bipolar depression, you are never sure when it will come to its conclusion or when you will reconnect with the world around you again.

Bipolar depression is not just sadness. It can feel like an emotional shutdown.

The Emotional Tug-of-War: Identity and Self-Worth

There is an internal emotional impact when you are experiencing a depressive state. A loss of identity and sense of self often come into play. You are more than sad when you are dealing with depression. You are in crisis and disconnected from everything and everyone around you.

I would often hear loved ones observe and say things like, “She’s not herself,” or “She is not full of energy like normal.” Even with the disconnection, you can still hear and feel, even if you cannot reason your way out of the depression. Statements like those have caused me to feel shame, guilt, and internal criticism.

I want to be the Onika everyone knows and loves, but I simply cannot. That is what many people who have never experienced long-term depression fail to understand.

Depression, low energy, low mood, staying in bed all day, insomnia, lack of appetite, low self-worth, loss of hope, and loss of sense of self are not choices. They are symptoms of a mental health condition. No matter what combination of symptoms I experience, they exist and have the power to change my identity.

When I discovered the concept of self-compassion years ago, I began practicing it during my depressive episodes. I realized that I am living with a severe mental illness characterized by both highs and lows. I cannot always dictate which one I experience or when, so I had to learn to show myself compassion and give myself grace.

If depression dictates that I will sleep all day, instead of forcing myself to move against it, I move with it. I make my bed as welcoming as possible because I am dealing with depression, and today, sleeping may be all I can do.

If I experience loss of appetite during an episode, the minute I feel real hunger, I eat something I truly love, like cheesecake for breakfast or a plate of pasta in the middle of the night.

I no longer worry about being the Onika everyone knows and loves because I recognize that I am still her. I am simply going through a human experience. Depression does not just change your mood. It can change how you see yourself, and I choose to see myself as someone who does not let depression define me or overtake me.

Instead, I move with depression until it is behind me, and I am able to move forward again in my journey to wellness.

Healing in the Darkness: What Helped Me Navigate It

It has always been difficult for me to communicate my needs to others while in a low state. Beyond ensuring that I am taking my medication or identifying the food I want to eat when my appetite returns, I have trouble articulating my wants and needs.

After so many years of having a solid support system in my family and friends, they are often more aware of my needs than I am. If I do not answer the phone after a few days, Grama Judie or my cousin will come by and check on me. Grama will tell me stories about the people in her life, and even though I am not really listening, she tries to make the connection.

My cousin will simply sit on my couch quietly, working away on a project while I sleep for hours at a time. The most he will say during a visit is, “You good? Do you need anything?” If I wave him off and growl, he just goes back to work. Sometimes he stays through the whole episode, and he always knows when I am coming out of it, when I start making my bed, signalling that the time to stay down is over.

When I am in a depressive space, it is really hard to write. I try to jot something down daily, whether it is the first two lines of a poem or a note about how I am feeling at that moment. My journal is never too far away.

At night, when my energy allows, I try to complete part or all of my nightly routine, which includes skincare, brushing my teeth, aromatherapy, and a grounding meditation. These practices usually happen when my mind is preparing to come out of the darkness, telling me it is time to start healing.

This is when I know depression is about to leave my body.

I have learned that it can disappear as quickly as it came, and I should always prepare for both its disappearance and its sudden reappearance. I have also learned to listen to my thoughts when they return. Whether they are telling me, “You need more sleep, Onika,” or “Go get something to eat right now,” I listen.

I know there is a period during my depressive episodes when the thoughts do not come, or they disappear too quickly for me to hear what they are trying to tell me. So when they return, and I can hear myself clearly, I listen.

Even in a low state, there are moments that slowly rebuild connection. The return of my ability to think clearly is one of them.

Final Thought:

Holding On When the Light Is Low

The return to myself starts with a glimmer of light. It is the light I see in my kitchen when I finally open my eyes and wake up from sleeping for a week. I turn my head toward the kitchen, and I do not immediately want to turn back to the darkness.

Then I lay there, staring at the low light, and I can hear myself thinking again. So I ask myself the question that always begins my return to me:

“Are you ready to get up and stay up?”

When the answer is yes, I begin my morning routine of bed stretching. I call out to Alexa to play CeCe Winans. I sit at the side of my bed, touch my heart, and thank God for getting me through.

I had to learn to trust that emotional states shift, high or low, over time. I had to trust that day one would come to an end, and day ten might be the day I am ready to get up.

In my experience, depression is about endurance, not resolution. Endurance with patience, self-compassion, and grace.

Since I was 16 years old, I have lived with some form of depression. I am 43 years old now, and I still experience severe symptoms. Depression is not going anywhere, so I had to place in my mind the ideas of sustain and withstand.

By definition, endurance means the ability to sustain prolonged physical or mental effort, withstanding hardship, stress, or fatigue to continue a task.

So, the only thing required of me was to endure, and I would survive depression?

I tried it, and it changed the course of this ongoing journey.

A big part of returning to myself was understanding who I became when symptomatic and who I am now that the depression has lifted. Holding on when the light is low means holding on to hope.

Hope that I make it through the storm.

Hope that there is sunshine after the rain.

Hope that I never give up.

Hope that I always reach for the light at the end of the tunnel.

Hope that I endure.

A Question to My Readers:

What helps you stay connected to yourself when everything feels distant or quiet inside?


Tuesday, May 12, 2026

When Worry Doesn’t Stop: Let's Talk about Generalized Anxiety Disorder and Its Overlap with Bipolar Disorder - Part 1

 

When Worry Doesn’t Stop: Let's Talk about Generalized Anxiety Disorder and Its Overlap with Bipolar Disorder - Part 1 of 5

Anxiety: The Worry That Lingers

I remember the exact moment anxiety entered my life. It was brought on by abject terror.

As a child, I had anxious moments when the anxiety-driven voices in my mind became so loud that I would have to shake my head a few times to quiet the noise. It felt normal, even manageable, until one spring afternoon outside my sixth-grade classroom when anxiety attacked me out of the blue.

To my recollection, here’s what happened.

The Day the River Threatened to Pull Me Under

It was the final few months of grade six, and everything seemed normal. We had just finished recess, and the playground was its usual discord of harshness, where bullies moved from group to group unleashing their cruel brand of humour on any kid who would listen, and especially on any kid they knew it would affect.

There was one boy in particular they reserved the worst of their venom for. That day, the boy, whom we can call Christopher, simply couldn’t take it. He let out a giant scream that echoed across the playground. Every kid stopped and turned to see where it was coming from.

It was coming from Christopher.

It’s still unclear how I got involved, but knowing me, I was always a champion of the underdog and went to his defence. I had a fixer personality even when I was young. Christopher did not seem to want me to fix things. I remember the angry look directed at me before he stomped off inside the school.

That afternoon, as I walked to my backpack cubby to get my notebook, I found a threatening letter instead. It read, “This will be you in five days,” with a disturbing drawing meant to frighten me.

That was the moment my mind began to race with thoughts of danger and death. My breathing became shallow, my vision blurred, and I collapsed on the hallway floor with the letter in my hand as my world fell off its axis and spun out of control. I remember my fingers going numb and taking on a distorted shape that can only be explained by the lack of oxygen moving through my body. My lungs felt as if they had stopped working, constricted in my chest, until eventually I could feel only the last shallow breaths I took before I fainted.

That is how my teachers and classmates found me. The ambulance and police were called once they realized what had put me in that condition. My vitals were checked, and I was given oxygen, although I still felt like I couldn’t breathe. My parents were called to take me home for the day to rest after my traumatic ordeal. It was promised to my family that the police would investigate and “get to the bottom of this.”

For the next two days, I stayed home from school. When I got home, my mother put me straight to bed, and that was when the anxiety and fear entered my sleep. I tried to rest but got very few hours, waking from nightmares of red walls and ropes tangling around me, squeezing the air out of me. My anxiety manifested as screams in the middle of the night. Screams that took my breath away. My stomach refused to hold down any meal, no matter how small. My head throbbed with agony, like a hammer beating against my brain, repeating the same rhythm over and over: “three more days until you die.”

My parents, being strict about school attendance, refused to let me stay home for the entire five days. So, on day four, I returned to school. I couldn’t concentrate. I sat at my desk in a state of hypervigilance. Sounds were too loud, lights were too bright, and my thoughts continued to spin out of control.

By day five, what I believed would be the final day of my life, I was a ball of anxious energy, no longer my cheerful, outgoing self. On that day, however, it was discovered by police and staff, after comparing handwriting samples from each student, that the culprit was Christopher. My parents were called in and told that he had behavioural problems at other schools and would be expelled as punishment for what he had done.

The punishment for me would be the beginning of a mental health condition I did not yet understand. I had no name for it, but I would experience it daily, living from anxiety attack to anxiety attack.

This blog is a reflection on my lived experience with anxiety. I will discuss living with both Bipolar disorder and Generalized Anxiety Disorder, also known as GAD, the challenges I have faced while trying to balance co-occurring disorders, and how changing my mindset helped me create a space where anxiety could exist.

This is the worry that lingers.

Some worry does not end. Instead, it loops, deepens, and stays.

When Anxiety Persists: A Bipolar Woman’s Reflection

After that incident, I started calling anxiety “the voices.” Throughout my adolescence, I would worry about anything and everything. I created scenarios in my head of negative events that were not actually happening and might never happen, but to my fragile mind, each scenario held some truth.

From the day I found that letter in my backpack, I lived in fear that something just as terrible would happen to me again. The sad part was that even my 11-year-old self knew it would be a hard road between me and regaining my peace of mind.

What I know now, that I did not know then, was that I would experience a series of life-changing events until one day I found myself in a child psychologist’s office being diagnosed with depression and a mild anxiety disorder. Mild anxiety would later develop into Generalized Anxiety Disorder as I got older and continued to struggle with processing painful experiences in a healthy way.

There is a difference between everyday concern and persistent anxiety. Persistent anxiety does not simply affect your thoughts. It also affects your perception of the world, your self-perception, your self-esteem, and your self-worth. Anxiety can even shape your behaviour.

It is not just persistent. Sometimes the worry that comes with anxiety is all-consuming.

Anxiety during a Bipolar manic episode is something I can only describe as loud and chaotic. Because one of the symptoms of mania is disorganized thinking, anxiety in mania can take on a disorganized, even paranoid form. In my experience, when Bipolar disorder occurs alongside anxiety, it can feel as if the extreme worry itself triggers hypomania, the precursor to mania.

When your body is in a constant state of fight, flight, or freeze because anxious thoughts persist day after day, your mind starts to break down. If you live with another mental health condition like Bipolar disorder, that internal pressure can increase the risk of a serious mood episode.

What Generalized Anxiety Disorder Feels Like: A Lived Experience Perspective

I moved to Toronto, Ontario at 33 years old to start working in the event management industry. I was fresh out of school when I was hired by a boutique events company where the staff consisted of myself, my boss, and another woman.

At first, things went well. I was securing big accounts, much to the excitement of my boss. Then one day, there was a notable shift between myself and my co-worker. She seemed to begin a passive-aggressive campaign to undermine my work and shake my confidence. She told me that if I did not find a way to bring in more clients, my boss would be forced to fire me.

That was the moment my anxious mind took control of my rational brain.

When you have Generalized Anxiety Disorder, unless you are experiencing visible physical symptoms or an anxiety attack, people cannot see the internal war you are fighting with your own thoughts. The moment I perceived that I could be terminated, I believed I was already terminated. The worry became persistent, excessive, and all-consuming.

I couldn’t eat or sleep because I was constantly thinking about being fired. Questions raced through my head one after another:

“When am I going to get fired?”

“What is my boss going to say to me?”

“How much time do I have left?”

“Should I start looking for another job?”

“Should I quit before he has a chance to fire me?”

“Should I just work harder to get the big accounts?”

“If I get the big accounts, will he still fire me?”

“Fired, fired, fired. You are going to get fired.”

With every thought came another and another. The thoughts, or voices, invaded my mind at work, and my performance declined. I started taking two and three days off so I could try to catch up on the sleep I was lacking, but also so I could isolate myself, untangle the anxious thoughts in my mind, and come up with a plan to keep my job.

I could not see how illogical I was being. Based on one person’s thoughtless comment, I was spiralling out of control.

I began to see danger around every corner, as if the world was not meant for me, as if I was not enough. There was nowhere I felt safe or secure, not at home and not at work. I eventually did get fired from that job, but I cannot blame my co-worker. She planted the seed, and I watered it with anxiety until the thoughts overwhelmed me.

Anxiety can feel like your mind is always preparing for something that has not happened. When something does happen, like me getting fired, anxiety can become deliberate, telling you your thoughts were right and that you have every reason to constantly worry.

Bipolar Disorder and Anxiety: When They Overlap

Trigger Warning: The below section discusses suicidal thoughts in a non-graphic way.

When you have a co-occurring condition like Bipolar 1 disorder and Generalized Anxiety Disorder, the emotional complexity can present as constant mental confusion and chaos. When you are in crisis, it is hard to tell where your thoughts end and anxiety begins.

During my depressive cycles, anxiety and the intrusive thoughts that come with it have sometimes deepened my distress and contributed to dangerous thoughts about my own life. For me, those moments often begin through the lens of anxious thinking, negative self-perception, diminished self-worth, and lowered self-esteem.

When depression shifts into hypomania, mania, or psychosis, my anxiety moves into that same realm of dysregulation and can take on a voice of illogical fear, paranoia, and emotional instability.

Anxiety has always felt different depending on my internal state. During remission or baseline periods, I have a firmer grip on my thoughts, and I can recognize more clearly when anxiety is trying to overtake me. I use tools like breathing exercises, meditation, and positive self-talk to calm the waves of anxiety that pass through me, attempting to pull me under into a dark place where my life has no value beyond what my anxiety dictates.

During episodes, however, it has always been difficult to distinguish mood shifts from anxiety symptoms. It becomes a constant question: which came first, the shifts or the symptoms?

When I reflect on my past experiences with Bipolar 1 disorder and GAD, I come to the conclusion that although Bipolar 1 disorder is my primary condition, Generalized Anxiety Disorder often acts as a trigger and causes my moods to shift.

For example, although I experience anxiety throughout the day, at night the voices often become louder and more persistent, disrupting my sleep. When I have insomnia for days at a time, when my thoughts will not quiet and prescribed medication does not have the desired effect, lack of sleep can lead to elevated mood and eventually mania.

Anxiety does not always stand alone. It often moves through mood states differently.

Living With Both: Emotional Weight and Exhaustion

There is an emotional fatigue that happens when living with overlapping mental health conditions, especially when each has its own dialogue inside your head. You become constantly alert, fearing relapse and living with uncertainty.

My past experiences with both conditions often creep into my present-day anxieties, especially when my mood shifts from elevated to low, or from low to elevated. The emotional weight and exhaustion of living with both Bipolar disorder and Generalized Anxiety Disorder can be overwhelming at times.

Then I remind myself that my mood disorder and GAD are both part of the lived experience that has shaped who I am today, both good and bad. Managing more than one internal experience can make even calm moments complex, but the calm moments, though rare, do exist.

At present, I practice self-awareness. When possible, I do not allow the voices inside my head to lead me. Instead, I show myself compassionate grace and remember that with inner strength and time, the voices can move from a loud roar to a dull silence.

I still hear and feel my anxiety when it creeps in, but with the self-care tools I have acquired, the emotional weight and exhaustion of living with anxiety has become less and less. It is not about ignoring my inner dialogue. It is about making space for it inside my head, a space where I can choose to listen to the anxious roar or turn it down to a dull silence I have learned to live beside.

Final Thoughts

Finding a Name for the Worry, Reclaiming Peace

Many years ago, the writer inside me decided to take control of the narratives in my head, the voices in my mind that I called anxiety. I realized one day, as I listened to the worry, that it often came in the form of a storyline. There would be one worrisome thought, and then that thought would build upon itself, creating a full story of anxiety.

Calling my worry one of the storylines in my head helped me untangle whether it was fiction or non-fiction, real or imagined. Although this has never been the solution to my anxiety, it was definitely a turning point in how I experienced it.

This new awareness created a space of understanding rather than a resolution to my condition. It allowed me to reflect on my ongoing relationship with anxiety.

Understanding anxiety does not end it, but it can change how you carry it.

To my readers: Have you ever experienced worry that felt constant or hard to quiet, and what helped you begin to recognize it for what it was?

Thursday, March 26, 2026

My Journey Through Madness: Writing, Reflecting, Re-Diagnosis, and Radical Honesty

 


The Page Became My Place of Survival

After nearly 20 years of navigating the highs and lows of Bipolar I disorder, I thought I understood the facets, complexities, and myriad shades of my illness. Then a new diagnosis, schizoaffective disorder, bipolar type with borderline traits, seemed to erase everything I believed I had learned. Over the past year, putting pen to paper has helped me live inside the latest version of my story. It has taught me how to love, learn, and accept myself as I rewrite a past I no longer recognize, a present where I am still searching for where I belong, and a future full of unknown possibilities.

This is not just a story of medical labels. It is a lived, raw, year-long journey of unraveling, discovery, grief, and creative survival. There were times when reflecting on the new diagnosis left me paralyzed by self-doubt, self-loathing, and defeat. There were other moments when I had to be radically honest with myself and ask: What does re-diagnosis change? In between those moments, I shed tears of grief over a lost identity, felt guilt over mislabelled lived experiences I had shared with the world, and struggled with disbelief over how broken I felt existing in a broken system. I had once believed I was thriving, yet suddenly found myself barely surviving.

This blog shares how one year of journaling, storytelling, and reflection helped me move through the chaos of re-diagnosis and into deeper self-awareness. I hope my journey through madness encourages you to reflect on your own experience of diagnosis or re-diagnosis so you can move from chaos to calm and continue your journey toward healing, recovery, and wellness, no matter the missteps or barriers that try to defeat you.

Bipolar I Disorder: Twenty Years in a Frame That Almost Fit

At 17 years old, I was assessed by a child psychologist. After that assessment, I was told I was experiencing generalized anxiety disorder and depression. No one told me that my journey through madness had begun that afternoon in a Scarborough hospital, in the office of “Dr. Glass,” the name I gave him because of his cold and clinical demeanor.

No one mentioned that anxiety and depression can sometimes be precursors to bipolar disorder, or that for many women, onset may happen in their mid-20s, often shaped by stress, trauma, and other precipitating factors. So at 17, I walked out of Dr. Glass’s office with my first mental health diagnosis, completely unaware that my mental health journey was beginning. I did not know there would likely be other diagnoses, misdiagnoses, and eventually re-diagnosis on my path toward wellness, emotional stability, and better health.

When I received my former and longest-standing diagnosis of Bipolar I disorder, I was 24 years old, just out of university, experiencing my first psychotic episode, my first hospitalization, and my first real initiation into the world of psychotic and mood-related disorders. The severity of my manic psychosis led clinicians to conclude that I was on the schizophrenia spectrum and other psychotic disorders, while also meeting nearly all the criteria for a manic episode, which formed the basis of a Bipolar I diagnosis.

So after the second mental health assessment of my life, I was placed in a frame, like a picture on a wall, with very few medical professionals noticing that the bipolar frame around the landscape of my mental health was off, crooked, leaning slightly the wrong way. It took 20 years of manic-psychotic episodes, hospitalizations, assessments, and reassessments for the mental health system to realize I had been misdiagnosed with bipolar disorder. The frame almost fit, but it did not capture the complex landscape of my mind or the combination of mental illnesses I exhibited both in and out of psychosis.

It was not until my most recent assessment at Ontario Shores Centre for Mental Health Sciences, where I was observed in one of their Complex General Psychiatry units, that psychiatrists realized my condition was not a simple one. Though I am still considered to be on the spectrum, the symptoms they observed, including auditory hallucinations, delusions, paranoia, and disorganized speech, did not fully align with the Bipolar I diagnosis I had carried for two decades. Instead, the new frame was called schizoaffective disorder, bipolar type with borderline personality disorder traits.

I would not learn about my re-diagnosis until a year after my discharge from Ontario Shores, but in truth, the discovery brought relief because in my heart the Bipolar I diagnosis felt true, until it did not. It was like being handed a giant blank canvas, with my new diagnosis as the uncomfortable centrepiece surrounded by empty space. With the support of my medical team, my personal support system, psychoeducation, psychotherapy, and my own willingness to keep moving forward, I began letting go of the old frame and working with a new canvas. I was able to reshape my mental health identity, create a more complete picture, and release a former bipolar disorder diagnosis that had almost, but not quite, explained everything in my symptom profile. Now it was time to move forward with a diagnosis that fit my experiences, both past and present, and changed the mental health landscape through which I viewed myself and my future.

Schizoaffective Disorder: The Diagnosis That Changed Everything and Nothing

What Is Schizoaffective Disorder?

Schizoaffective disorder is a chronic mental health condition that combines symptoms of schizophrenia, such as hallucinations, delusions, or disorganized speech, with a major mood disorder, either depression or bipolar disorder. It involves both psychosis and severe mood symptoms, and it typically requires a combination of medication and psychotherapy for long-term management.

There are two main types of schizoaffective disorder. Bipolar type includes episodes of mania and sometimes depression. Depressive type includes only major depressive episodes. One of the key features that distinguishes schizoaffective disorder from other psychotic disorders is that psychotic symptoms must be present for at least two weeks without prominent mood symptoms.

Unlike bipolar disorder, schizoaffective disorder often involves persistent psychosis or delusions outside of mood episodes, which can lead to significant functional impairment. There is no known cure, but the condition can be managed through medication, including antipsychotics and mood stabilizers, as well as psychotherapy and ongoing support.

A Newly Diagnosed Woman’s Reflection: The Emotional Impact of Schizoaffective Disorder

Going from bipolar to schizoaffective in what felt like mere seconds, the day I discovered the new diagnosis while reading my social worker’s assessment notes from February 4, 2024 in my medical records, was more than a shock. It was life-shattering. I went from being a 42-year-old woman with a 20-year history of Bipolar I disorder to someone recently re-diagnosed with schizoaffective disorder, bipolar type with borderline traits.

As I read the notes and tried to interpret their meaning, I could feel my mind pressing against my skull, my ears ringing, and my palms turning clammy with sweat. It was as if my world stood still, yet the ground beneath my feet had become unstable. With every word, my mind screamed in disbelief as the sound of my tears filled the still silence of my living room. For the first time since my mental health journey began, I felt truly alone.

Shame, confusion, betrayal, and fear washed over me like summer rain. But there was something else hidden in the recesses of my mind, fighting to come through, an emotion demanding acknowledgement through the shock and grief: reluctant relief. For 20 years, I had lived in a space of the unknown. Unknown symptoms that did not fit the bipolar profile. Chaotic psychotic episodes experienced without any real explanation. A diagnosis psychiatrists believed was the key to treatment and management. And beneath it all, the constant questions: What is wrong with me? Why does a diagnosis I have carried for two decades feel wrong with every episode I have? The answer, painfully, was because it was.

When I was 24 years old, a doctor labelled me based on one episode and a handful of DSM criteria, and ever since that day I was never entirely comfortable in my bipolar identity. I simply did my best to make it work. Relief quickly turned into grief over losing an old narrative, and anxiety over embracing a new one. I had fully embraced bipolar disorder, but could I now embrace schizoaffective disorder, especially when it came with equally complex elements of bipolar type and borderline traits? Could I begin a new journey of self-discovery, a new journey toward women’s mental health, healing, and recovery, and leave the baggage of old labels behind? Only time, along with self-compassion, self-love, and deep self-reflection, could begin to answer the many questions that came with my new diagnosis.

Writing: My Mirror, My Map, and My Medicine

After discovering my misdiagnosis and new diagnosis of schizoaffective disorder, I felt lost, so I did the only thing I knew how to do to find my way again: I began to write. I had been writing through mental illness, through all the ups and downs and every moment in between, from the very beginning of my journey. I have journals and hand-crafted notebooks, some gifts from people who love and understand my struggle, others just loose-leaf pages requested behind the walls of psychiatric units and filled with psychosis-driven thoughts. Writing daily became a ritual, one that has always helped me find my way back to myself and back to sanity. Journaling for mental health clarity has always brought me comfort in the chaotic world psychosis creates around me.

When I journal through the various stages of illness, depression, hypomania, mania, and psychosis, it becomes a record of my mental growth and progress. When I finally reach the light at the end of an often very dark tunnel, I have the opportunity to look back and reflect on the different voices that come through me as I move from illness back to baseline and wellness. The patterns in my language, the themes and tones of my daily writing, even my penmanship, all serve as indicators of my thought process and illness progression in ways therapy simply cannot always catch in a one-hour daily or weekly session.

There is therapeutic value in storytelling, even when it is done in madness, while healing from symptoms that make you lose yourself. When I write, no matter the stage, I have always been able to find my way back to baseline, back to wellness, and back to me. Writing has become my map, my mirror, and a form of medicine. It has supported my resilience, strengthened my self-awareness, and given me a structure and routine to return to when everything else feels uncertain.

Final Thoughts

One Year Later: What I Know Now That I Didn’t Then

Living with schizoaffective disorder has been an education. My new diagnosis has presented many challenges, especially the resistance I still feel when I share it with others. I still have a habit of cutting myself off before I speak of the type and the traits because I am still discovering what they mean within my symptom profile. What I have accepted is that schizoaffective disorder is not just a label. It is an invitation to see myself and reflect on my experiences more fully. Though I felt broken a year ago when I discovered my re-diagnosis, today I feel more honest and more authentic in my experiences and in my journey through madness toward wellness. My mental health recovery has been shaped in large part by writing, which has taught me that I do not need to be “stable” to be whole.

Reflecting through writing has strengthened my resilience, self-compassion, self-acceptance, self-love, and ultimately my self-awareness. This past year was not just about surviving a re-diagnosis. It was about reclaiming my voice, one word at a time. Writing did not cure me. It witnessed me. And sometimes that is what healing looks like.

To my readers, take this question with you on your own journey toward healing and women’s wellness, as I have carried it with me over the past year and beyond:

What if madness isn’t the end, but the beginning in disguise?

Monday, March 23, 2026

When the Voices Didn’t Match the Diagnosis: Hearing Voices with Schizoaffective Disorder

I Thought It Was Just Stress, Until the Voices Stayed

For years I was told hearing voices was a symptom of the mania I experienced with Bipolar I disorder. I accepted that. But the voices I heard during calm moments did not fit. They whispered in between episodes, in the quiet. Eventually, someone listened long enough to give it a name: Schizoaffective disorder.

Schizoaffective disorder is a complex mental illness that blends Schizophrenia symptoms with a mood disorder, in my case Bipolar I disorder. Since childhood, I can remember hearing voices in my head that made little sense. At times they were muffled, more like noise in the recesses of my brain than clear speech. During stressful periods, they grew louder and sharper, delivering messages that questioned my self-worth and chipped away at my confidence.

Hearing voices can feel terrifying, isolating, or strangely familiar. It becomes even more confusing when your diagnosis does not fully account for it. When I was first diagnosed with Bipolar I disorder, I believed the voices were simply a symptom my medication was not strong enough to quiet. To be fair, I had lived with them so long they felt woven into my mental landscape. I trained myself not to question them and, for the most part, not to acknowledge them.

At their worst, the voices guided impulsive and disruptive behaviour, sometimes through religious ideation. At best, they were static in the background, white noise I could ignore. This blog explores what it is like to live with auditory hallucinations through the new lens of Schizoaffective disorder after years of living under a Bipolar I diagnosis.

The Voices That Didn’t Wait for Mania or Depression

Auditory Hallucinations: Bipolar Disorder vs. Schizoaffective Disorder

Auditory hallucinations in Bipolar disorder with psychotic features usually occur only during severe manic or depressive episodes and tend to resolve once the mood episode ends. In Schizoaffective disorder, hallucinations can persist for at least two weeks outside of a mood episode, which reflects a more chronic psychotic profile.

In Bipolar disorder, hallucinations often match the mood state. During depression, they may attack your self-worth. During mania, they may feed grandiosity or urgency. In Schizoaffective disorder, hallucinations are more independent of mood and can continue even during relatively stable periods. They may also feel more chronic, more intrusive, and less tied to a specific emotional state.

I learned early in my mental health journey that hallucinations, whether auditory or visual, were only supposed to happen during psychotic episodes. My reality, however, has always been different. I hear voices during periods of stability as well as during stress and crisis. They are not always constant, but they are familiar. Until recently, that left me feeling disconnected from my original Bipolar I diagnosis because the criteria did not fully reflect what I had been living with for most of my life.

Though I had grown used to hearing voices and learned to block them out, I could not explain where the symptom was coming from or how to gain the right tools to cope with auditory hallucinations that seemed to follow me regardless of mood.

The Moment It Made Sense, And Still Hurt

Everything changed for me when I discovered the Schizoaffective disorder diagnosis. I knew very little about the condition except for a few patients I had met during past psychiatric residencies. I remember one young man explaining that he constantly heard voices or noise in his head, sometimes giving him instructions, and that he had learned not to obey them. He said, “Just because they’re there doesn’t mean I have to listen.” That stayed with me.

My own voices often attack my self-worth and amplify everyday fears during periods of stability. When I am unwell, they shift and become darker, leaning toward suicidal or religious ideation.

During my residency at Ontario Shores Centre for Mental Health Sciences, I underwent a psychiatric re-evaluation and my diagnosis changed. While I did exhibit symptoms of Bipolar I disorder, deeper observation brought to light symptoms that had previously been overlooked, especially the continuous and intrusive auditory hallucinations. When I stumbled upon my new diagnosis of Schizoaffective disorder, bipolar type, I felt many things at once. I felt grief, confusion, and anger. But I also felt relief. At last, I had a diagnosis that included all of me, all the symptoms that had gone unexplained and untreated for years.

Still, I mourned the loss of my old diagnosis. For more than twenty years, Bipolar I disorder had framed my experiences, my advocacy, and the way I understood myself.

The question I kept asking was simple and painful: How am I supposed to move forward on my journey to wellness if I do not even know my diagnosis? How am I supposed to navigate this world if I do not know what I have?

It was my support team that reminded me that a diagnosis is a label, not my identity. They let me grieve, but they also reminded me that new information is not a punishment. It is a tool.

Living with Voices, Not Just Silencing Them

The most valuable lesson I have learned while managing auditory hallucinations, long before Schizoaffective disorder was formally added to my mental health profile, is that I am still in the driver’s seat. Not all voices are commands. In my experience, they are often commentary, echoes, or emotional mirrors that feed fear and anxiety into my mind.

Instead of feeding the noise, I have learned to interrupt it. A few things help me:

Practice grounding techniques.

Breathing exercises, meditation, and hikes in nature help regulate my body and redirect my focus. Nature’s sounds can be louder and clearer than the noise inside my head.

Listen to music, often.

I have found that I cannot fully absorb two things at once. When I listen to artists like CeCe Winans, Drake, Ne-Yo, Ella Fitzgerald, or my gospel and 90s alternative playlists, my mind fills with memories, comfort, and emotional safety instead of fear.

Adjust medication when needed.

Once my psychiatrist and I began openly discussing the voices, we were able to adjust my medication in a way that improved my external focus rather than leaving me trapped in my inner dialogue.

Talk about the experience.

I speak with at least one member of my support team every day. Whether I am sharing anxiety, receiving prayer, or hearing encouragement, that connection helps me cope with voices that can feel loud, negative, and overpowering.

Coping with voices when you live with Schizoaffective disorder is not easy, but it is possible. Talking about them instead of pretending they are not there was one of the first steps in taking away their power. The more honestly you share your lived experience, the less likely shame and stigma are to define it. This is your journey, and you get to choose who you share it with. But there is support in families, communities, peer spaces, and professional care if you are willing to reach for it.

Final Thoughts

Reclaiming Power Through Understanding

People say knowledge is power. I believe knowledge also brings understanding. When it comes to auditory hallucinations, no two experiences are exactly the same. That is why safe spaces matter. Whether in peer support, therapy, or a hearing voices group, being able to speak honestly about what you hear can shift the experience from fear to understanding.

Voices may be part of your condition, but they are not your identity.

The more I understand what I experience, the less power those voices have over me. And that, in itself, is a form of healing.


Thursday, February 12, 2026

When the Diagnosis Changes: Living Through a Shift from Bipolar I to Schizoaffective Disorder

When the Diagnosis Changes: Living Through a Shift from Bipolar I to Schizoaffective Disorder

After Twenty Years Everything Shifted

For almost two decades, I shaped my identity, routines, and survival around being someone with Bipolar I disorder. Then one day, after another hospitalization and a deeper evaluation, I was re-diagnosed with schizoaffective disorder, bipolar type, with borderline traits. The experience left me feeling off balance.

What shook me most was not only the discovery of the new diagnosis, but the lack of communication from my care team. In mental health care, there is often a strong focus on stabilization and symptom management, while psychoeducation and transparency are left behind.

In my case, the diagnosis change occurred during my residency at Ontario Shores Centre for Mental Health Sciences. I was still deeply in my illness when it was presented during a clinical case conference, delivered in medical language without explanation. No one took the time to help me understand what this shift meant for my treatment, medication plan, or future as someone now living with a different diagnosis.

A new diagnosis after living so long under a familiar label can feel like losing your footing. Yet it can also bring clarity, relief, and the opportunity to rebuild. It invites reflection on the past, intention for the present, and planning for the future with honesty rather than fear.

This blog is a deeply personal look at what it means to be re-diagnosed after years of living with Bipolar I disorder, how that shift impacted my sense of identity, and what I learned from beginning again with a new language for my mental health.


The Diagnosis That Defined Me for a While

For nearly twenty years, Bipolar disorder became my identity. It was the lens through which I understood my moods, my choices, and my challenges. At first, I resisted it. Later, after learning to manage my illness, I came to call it my superpower. I even tattooed the word Bipolar on my left forearm as an act of defiance in a world that misunderstood what living with this condition truly meant.

There was duality in that identity. During manic and psychotic episodes, I felt euphoric and fearless, as though past trauma could no longer touch me. I believed I was unstoppable. Yet those same episodes led to destructive decisions, strained relationships, and repeated hospitalizations marked by isolation, loss of autonomy, and deep emotional loneliness.

Still, familiarity offered comfort. After fourteen hospitalizations, I knew my bipolar cycle well. Anxiety and depression would arrive first, often triggered by trauma, stress, or insomnia. Hypomania followed with excessive energy, impulsive spending, and risky behaviors. Eventually, mania and psychosis would take over, ending in hospitalization. This cycle became my normal.

Looking back now, I can see there were signs that something did not fully fit the bipolar framework. There were symptoms that lingered outside mood episodes, pieces of my experience that never quite aligned with the diagnosis I carried as my identity.


The Day Everything Changed

I remember with startling clarity the day everything shifted. I had just begun a trauma informed treatment program through Ontario Shores and was required to complete weekly questionnaires through the hospital portal. For the first time, I was granted access to my medical records.

Out of curiosity, I began reviewing past psychiatric notes, assessments, and daily reports written during my residency. Then I opened a psychosocial assessment dated February 2, 2024.

It read:

Ms. Onika Dainty is a 41 year old woman with a diagnosis of schizoaffective disorder, bipolar type, with noted borderline traits.

I read it once. Then again.

My first thought was disbelief. Then anger followed. I was almost a year out of hospital and this was the first time I had seen this diagnosis. Questions flooded my mind. Why was I never told? How many people knew? How was I supposed to move forward if I did not understand what I was living with?

At that moment, what little trust I had in the mental health system fractured. I reached out to my support circle in tears, mourning the loss of an identity I had carried for twenty years.

My cousin and Grama Judie reminded me of something grounding. Nothing about me had changed. The diagnosis was words on paper. I was still Onika, still resilient, still equipped with tools that had carried me this far.

When I met with Dr. A, my outpatient psychiatrist, he acknowledged that he had been aware of the diagnostic shift. He explained the reasoning behind it. My prolonged psychosis outside mood episodes, treatment resistance, and complex symptom presentation during my residency had led clinicians to re-evaluate my diagnosis.

Suddenly, pieces that never fit before began to make sense.


Grieving, Reframing, and Relearning

It has been nearly a year since discovering my diagnosis of schizoaffective disorder, bipolar type, and I am still learning how to hold it. Processing a diagnosis change requires grief. I had to mourn the identity I built around Bipolar disorder, reframe familiar pain with new language, and unlearn the stigma attached to a condition I once feared.

In 2019, I publicly advocated for Bipolar awareness through national campaigns, interviews, and speaking engagements. I proudly told my story as a Caribbean Canadian woman living with a severe mood disorder. I often said Bipolar disorder was my superpower.

Learning that I had been misdiagnosed shattered me. I questioned how I could have built a platform, a voice, and a sense of purpose around something that was never entirely accurate. I felt like an imposter frozen in uncertainty.

Grief followed its familiar stages. Denial gave way to anger. Bargaining convinced me that schizoaffective bipolar type still meant I belonged in the bipolar category. Depression left me immobilized. Acceptance came slowly.

What I ultimately realized was this: the failure was not mine. The failure lay in a system that prioritizes crisis stabilization over patient education and informed consent.

Once acceptance arrived, I returned to what has always grounded me. Education. I studied the DSM 5, read everything related to schizoaffective disorder, and finally saw my lived experience reflected clearly. Symptoms that once confused me now had context. Knowledge gave me power and peace.


Final Thoughts

You Are Allowed to Evolve, Even in Diagnosis

After more than twenty years of living with severe mental illness, I carry invisible battle scars. I have learned painful lessons and received unexpected blessings. Perhaps I was not meant to learn of this diagnosis while still fragile and newly discharged. Perhaps I needed stability first in order to receive truth without collapse.

Today, I believe this diagnosis was not the end of my journey but an evolution of it. I was never broken, only misunderstood. When treatment finally aligned with the truth of my experience, my healing deepened.

My mental health diagnoses are part of my story, but they are not the entirety of who I am. Identity, like healing, is fluid. It changes as we grow, learn, and survive.

A new diagnosis does not erase your past, your progress, or the strength it took to reach baseline. It simply clarifies the path forward.

To my readers:
Have you ever had to let go of an identity in order to step closer to the truth of who you really are?