Thursday, April 9, 2026

From Patient to Panelist: A Reflection After the 2026 SPA Convention (The Society for Personality Assessment)

From Patient to Panelist: A Reflection After the 2026 SPA Convention
(The Society for Personality Assessment)

 From Patient to Panelist: Entering the Room

As I walked through the doors of the Sheraton Centre Toronto Hotel for the 2026 SPA Convention, I felt a quiet anticipation for what the morning would bring. I had been invited to join the LEAF Deep Dive Panel only days before, yet even as a late addition I knew I was meant to be there.

The panel focused on psychiatric assessments. It explored what it means to seek assessment, move through the process, and live with the outcome of a diagnosis.

After more than twenty years as a patient within the mental health system, I had experienced assessment, reassessment, diagnosis, and misdiagnosis. My voice had echoed through psychiatric units across Ontario. Now, as I entered the Huron Room, I stepped into a space that patients rarely access.

I carried both apprehension and purpose. I was determined to share my lived experience with clinicians, researchers, educators, and thought leaders responsible for shaping the very systems that had shaped my life. I wanted to know whether lived experience truly belonged in professional spaces.

This blog reflects on that experience. It explores what it means to move from patient to panelist, and the impact of being invited into rooms where mental health systems are discussed, evaluated, and reimagined.


Surrounded by Leaders Shaping the Mental Health System

The energy in the Huron Room was thoughtful and uncertain. There was a quiet divide between healthcare professionals and lived experience panelists. We were all there for the same reason, yet there was a sense of curiosity about what would be said and whether it would lead to meaningful change.

As each panelist shared their story, a common message emerged. The mental health system must do better when it comes to psychiatric assessments. For many of us, including myself, the assessment process shaped the course of our lives. Diagnoses determined treatment plans, medication, and long-term mental health management.

We emphasized that assessments are the first line of defence in mental health care. When done incorrectly, patients carry the consequences through misdiagnosis, ineffective treatment, and prolonged suffering.

Looking out at the audience, I could see the shift. What once may have felt routine or procedural began to take on weight. Assessments were no longer checklists. They became human experiences with lasting impact.


From Subject of Assessment to Contributor to the Conversation

After years of psychiatric assessments that often led to hospitalization, I felt a deep sense of pride standing in front of that room. For the first time, my experience was not being documented. It was being heard.

My lived experience was no longer data for observation. It became insight for change.

Moving from subject to contributor was a powerful shift. I felt seen not as a diagnosis or case history, but as a person with knowledge, perspective, and something meaningful to offer. My journey, with all its complexity, had purpose beyond survival.


Entering the Rooms: A Panelist’s Reflection on a Rare Experience

Being invited into a professional conference space like this is rare for someone with lived experience. These are rooms typically reserved for clinicians, researchers, and decision makers.

I never imagined that my mental health journey would lead me from being assessed to participating in conversations about how assessments should be done.

That access felt like a gift. What was once a system I struggled to navigate became something I could begin to understand. The walls that once felt impossible to cross were no longer barriers.

After more than fourteen psychiatric assessments, multiple hospitalizations, and experiences of restraint and isolation, standing in that room felt transformative. My voice, once confined to clinical settings, was now part of a broader conversation.

Sharing my story allowed it to become something larger than myself. It became part of a collective understanding that could shape future care.


Unrestrained: The Emotional Impact of Being Seen

During the panel, I was asked to speak about my personal experience with psychiatric assessments.

My response was honest and deeply emotional.

I shared how most of my assessments occurred under duress. They often began with a wellness check by police, followed by apprehension, transport to hospital, and placement under observation. I described the isolation, the restraints, and the lack of autonomy that defined those experiences.

For the first time, I spoke openly about what that process felt like. Not as a clinical case, but as a human experience.

As I spoke, I felt something shift. I felt unrestrained. I was no longer being observed. I was being heard.

The tears that followed were not just about pain. They were about release. They were about finally being seen.


The Impact of Psychiatric Assessments: A Message to SPA Professionals

After years of assessments and over two decades of living with mental illness, I was still misdiagnosed for much of that time. That reality points to a larger issue within the system.

It was not until my residency at Ontario Shores Centre for Mental Health Sciences that I received what I believe to be a more accurate diagnosis. Even then, communication remained a challenge. I discovered my diagnosis through medical records rather than direct conversation.

This highlights a critical gap in mental health care. There is often a disconnect between clinicians and patients. Clinicians focus on diagnostic criteria, while patients seek understanding, clarity, and tools for living.

Resources like the DSM 5 provide diagnostic frameworks but offer little guidance on how to live with a diagnosis. Patients are left to build their own systems of care through trial, error, and personal resilience.

For me, that system includes self-advocacy, therapy, medication management, sleep hygiene, nutrition, exercise, and self-care practices such as journaling and reflection.

When patients leave the hospital, they are often given minimal guidance. Yet they are expected to navigate a complex mental health system on their own.

Diagnosis is only the beginning. It is not the end of the journey.


Final Thoughts

How Understanding Can Lead to Change: A New Sense of Possibility

After the panel ended, clinicians and attendees approached me with gratitude, curiosity, and a desire to stay connected. Some did not know what to say beyond thank you. Others expressed how impactful it was to hear lived experience directly.

One psychiatry student shared that my voice brought awareness into spaces where it is often missing.

That moment stayed with me.

Being in that room was not just about visibility. It was about contribution, connection, and reclaiming a voice in spaces that shape real lives.

My hope is that experiences like this create more opportunities for lived experience voices to be included in mental health conversations. These voices have the power to move us beyond stigma and toward meaningful change.

Being in the room did not erase my past. But it changed what felt possible for my future.

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?

Monday, January 12, 2026

A Complex Storm: Understanding a New Diagnosis of Schizoaffective Disorder

A Complex Storm: Understanding a New Diagnosis of Schizoaffective Disorder

A Diagnosis I Didn’t See Coming

It was January 2025 when I started a group trauma informed treatment program at Ontario Shores Centre for Mental Health Sciences. For the first time in the history of my mental illness, I was given access to my personal medical records from my stay at the psychiatric hospital. I was curious about what the medical staff, social workers, psychotherapists, and psychiatrist had observed while I was deeply unwell during my three month residency in 2024. When I began exploring the daily, detailed reports about my behaviour and activity on the unit, nothing seemed out of the ordinary. It all appeared to fit my experience of mania and how I remembered behaving.

Then I opened a Psychosocial Assessment dated February 2, 2024, and something shifted inside me. It felt like the identity of my illness had changed, and with it, the way I had understood myself for over 20 years. The report read:

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

The ground beneath my feet shook. I knew it was not a medical error. I felt confused and betrayed, but also like I had just been handed another piece of the puzzle that makes up my complex mind. I knew very little about this diagnosis, yet I was determined to face it head on.

Being newly diagnosed with schizoaffective disorder can feel overwhelming, isolating, and hard to explain, even to yourself. This blog explores what schizoaffective disorder is, how it overlaps with diagnoses like bipolar disorder, and what it can mean to live with a layered mental health condition.

What Is Schizoaffective Disorder? A Blended Symptom Profile

What is Schizoaffective Disorder?

Schizoaffective disorder is a complex mental illness that blends symptoms of schizophrenia, such as hallucinations, delusions, and disorganized thinking, with symptoms of a mood disorder, such as depression or mania. This combination can disrupt thoughts, emotions, and daily functioning. There are two main types: bipolar type and depressive type. It is often misdiagnosed early because the symptom profile overlaps with both schizophrenia and mood disorders like Bipolar disorder.

Schizoaffective vs Bipolar vs Schizophrenia

Schizoaffective disorder is a hybrid condition with a blended symptom profile. Schizophrenia and Bipolar disorder have distinct clinical categories, with schizophrenia typically defined by psychosis and Bipolar disorder defined by episodic mood shifts. The overlap becomes especially confusing when someone experiences manic psychosis and continues to have psychotic symptoms after the mood episode begins to stabilize. In other words, the mood may calm down, but hallucinations, delusions, or disorganized thinking can linger beyond the manic phase.

The Emotional Weight of a Complex Diagnosis: A Formally Bipolar Woman’s New Blended Reality

The biggest challenge I faced with my new diagnosis of Schizoaffective disorder-bipolar type, was the feeling of being misled by my medical team. I was almost a year out of hospital when I discovered it. If I had not been curious enough to read my medical reports, I would have continued living under a label that no longer fit the full picture of my mental health.

I was angry, ashamed, and afraid. The moment I read Schizoaffective disorder in my file, I felt like I had lost my identity. I felt like I had walked down the wrong path on my journey to wellness and that I was too far in to turn back and start over.

And yet, there was also relief. I had always felt pieces of my mental health puzzle were missing. When I am in psychosis, I have experienced auditory delusions, visual hallucinations, and extreme disorganized thinking. My Bipolar disorder framework could not fully explain those symptoms, so I told myself they were simply part of my manic episodes. After being in and out of psychosis for almost a year, unable to manage on my own, admitted and discharged from units whose main mandate was to stabilize me, I eventually became a resident of a mental health hospital with the time and resources to observe me properly.

When I saw the new diagnosis, I thought I should feel gratitude, but instead I mourned. I mourned the woman who had fought for almost 20 years against stigma, discrimination, and misunderstanding related to Bipolar disorder. I became an advocate, a peer support specialist, and a woman who learned the language of mental health so I could move through a world that often saw me as broken. How would I keep moving forward if I did not even know what I had? If my care team was not being transparent with me?

That evening I called my cousin in tears, and he asked me a profound question: Are you a different person than you were yesterday? Are you still the woman who has the tools to manage your mental illness, regardless of what it is called?

The answer was a resounding yes. My diagnosis had changed, but I had not. I was still Onika. I was still determined. My goal has always been healing, emotional stability, and a full, joyous, robust life. Nothing changed except that I now had a more complete picture of my symptom profile. I had to let go of the person I thought I was, close the door on the diagnosis I believed was mine, and make space to learn and grow within this new blended reality.

Learning to Manage the Dual Sides of the Diagnosis

Once I moved through the initial shock of my Schizoaffective disorder diagnosis and began educating myself, I was able to take my power back and rebuild a management strategy that spoke to all parts of my mental health. I started by looking at treatment options and realized they were similar to what I already knew. A combination of antipsychotics, mood stabilizers, and psychotherapy was recommended by my mental health care team.

Since my discharge from Ontario Shores Centre for Mental Health Sciences in 2024, I have not experienced psychotic symptoms, but I have noticed longer mood shifts. I track these mini episodes in my daily planner because structure and self awareness help me stay grounded.

Managing Schizoaffective disorder has its challenges, but I prioritize routine, healthy habits, and stability as a form of protection. Sleep hygiene has become a primary pillar of my care plan. I am still a 5 a.m. person, but now I take my medication earlier so I can get eight to ten hours of sleep consistently. My second pillar is stress management. I use meditation, breathwork, and daily movement to reduce anxiety and support emotional regulation. My third pillar is medication adherence and transparency with my healthcare team. I take my medication as prescribed and check in monthly, or sooner if I feel a crisis on the horizon. The final pillar is self care, self compassion, and grace.

I feel brand new in this diagnosis, so I keep reminding myself that once upon a time I was new to Bipolar disorder too. I felt helpless and alone then. Over time, I learned to advocate for myself. I learned to lean on my support team. I learned that healing is a process, and that psychoeducation, routine, and community can hold you steady when your mind feels loud.

Final Thoughts

It’s Okay to Be in the Process

With this new diagnosis, I have had to accept a few hard truths. First, it is okay to be in the process, as long as I am an active part of the process. This diagnosis is part of my reality, but it is words on a page in the next chapter of my life, not the entire book and not how my story ends.

I have also learned to stop chasing the “right” label and start listening to my lived experience. Schizoaffective disorder is simply terminology for a cluster of symptoms I have always carried. In many ways, it is not a detour. It is a more accurate map for the journey I have already been on.

Whether it is Bipolar disorder, anxiety, PTSD, ADHD, or Schizoaffective disorder, I have always fought for a better life while living with mental illness. None of these labels define me. They guide me toward understanding the unique, and often beautiful, trappings of a complex mind.

To my readers: If a diagnosis could be a doorway instead of a definition, what kind of understanding might you find on the other side?

Monday, January 5, 2026

More Than One Storm: Managing ADHD with Other Mental Health Diagnoses | Being Diagnosed with Multiple Disorders - Part 3

 

More Than One Storm: Managing ADHD with Other Mental Health Diagnoses

Being Diagnosed with Multiple Disorders - Part 3

I Thought It Was Just Anxiety, Then Came ADHD

For years, I blamed my forgetfulness, restlessness, and impulsivity on anxiety or mood swings. Then came the ADHD diagnosis, and suddenly the pieces clicked into place.

Since childhood, I lived with a relentless internal dialogue. The noise in my head only quieted when I shook it hard, almost violently, as if resetting my brain. That internal monologue followed me into adulthood. When I was diagnosed with Bipolar I disorder, I explained the noise as part of bipolar symptoms that intensified during episodes and lingered during anxiety or stress, even in remission.

Although I was prescribed medication to stabilize my mood, manage psychosis, and treat anxiety and PTSD, the constant mental chatter never fully stopped. It was not until my hospitalization in 2023 that a hospital pharmacist raised the possibility of co-occurring Attention Deficit Hyperactivity Disorder (ADHD). He explained how ADHD often goes undiagnosed in people with Bipolar disorder because stabilizing severe mood symptoms takes priority. He encouraged me to pursue testing.

When I finally spoke to my psychiatrist, he agreed. The results were clear. I was diagnosed with ADHD alongside Bipolar I disorder.

Living with ADHD alongside Bipolar disorder, anxiety, or PTSD adds complexity, but it also brings clarity when understood in context. This blog explores how ADHD shows up in people with multiple diagnoses, how to distinguish overlapping symptoms, and how to manage them with compassion, structure, and self awareness.

What ADHD Really Looks Like, Especially in Adults with Other Diagnoses

ADHD in adults often presents as chronic inattention, disorganization, difficulty with focus, time management challenges, missed deadlines, and losing items. Hyperactivity may look like restlessness, constant motion, or feeling unable to slow down. Impulsivity can show up as interrupting, impatience, impulsive decisions, mood shifts, or emotional outbursts. These symptoms affect work, relationships, and daily functioning, and they are often rooted in childhood experiences or trauma.

ADHD, Bipolar disorder, and Anxiety disorder share overlapping symptoms including impulsivity, irritability, distractibility, restlessness, and sleep disruption. This overlap can make diagnosis challenging. ADHD symptoms tend to be persistent and consistent, while bipolar symptoms are episodic, cycling between mania and depression. Anxiety is characterized by excessive worry, but all three conditions share emotional dysregulation and focus difficulties.

Because Bipolar disorder is severe and volatile, its symptoms are often treated first, which can delay ADHD diagnosis. ADHD is a neurodevelopment disorder that affects executive function, emotional regulation, self control, and attention. Anxiety disorders exist as a separate category but frequently co-occur with both Bipolar disorder and ADHD, creating symptom masking that complicates diagnosis.

Historically, Black women, neurodivergent adults, and trauma survivors have experienced delayed or missed diagnoses. Ongoing self monitoring and transparent communication with mental health providers are essential for accurate diagnosis and effective treatment.

Untangling the Threads: ADHD in a Multi Diagnosis Life

Living with multiple mental health diagnoses requires understanding how each condition shows up in your body and mind. When I received my ADHD diagnosis in 2024, I felt both overwhelmed and relieved. I have a research oriented mind, so I immersed myself in psychoeducation, peer support, and medication information. Over time, I gained clarity about how ADHD fits into my symptom profile.

For years, I attributed my impulsivity solely to manic episodes. While mania intensifies impulsive behaviour, I learned that ADHD driven impulsivity is chronic and rooted in executive function challenges. Manic impulsivity is episodic and driven by mood disturbance. Recognizing this distinction helped me manage one of my most difficult symptoms with greater self compassion.

Understanding this difference allowed me to build routines, structure, and healthy habits that prepare me for both ADHD related impulsivity and bipolar mood shifts. I learned to check in with myself and my support team, remain transparent with my healthcare providers, and ask for help early.

I also learned to distinguish between depressive episodes and ADHD related executive dysfunction. There are times when my body shuts down completely. I feel no sadness, just profound exhaustion and mental blankness. Rest and sleep regulation are the only remedies. Other times, emotional overwhelm and depressive inertia take hold. During those periods, I lean on my support system and remind myself that bipolar depression will pass with effort, care, and time.

Identifying whether a challenge stems from ADHD or Bipolar disorder helps me respond with the right tools and protects my overall mental health.

Strategies That Work for ADHD, Even When You’re Managing Other Disorders

Managing ADHD alongside other diagnoses requires an integrated and personalized treatment plan. In my experience, the most effective approach combines medication management, psychotherapy such as Cognitive Behavioural Therapy (CBT), and lifestyle strategies centred on structure, routine, and healthy habits.

Working collaboratively with psychiatrists and therapists ensures comprehensive care. Treating the most impairing condition first often reduces symptoms across diagnoses. The tools I developed to manage Bipolar I disorder became invaluable when ADHD entered the picture.

Daily structure supports my stability. I rely on planners, to do lists, timers, medication reminders, and consistent sleep hygiene. I break tasks into small steps, schedule rest intentionally, and use energy peaks wisely. Digital tools like Todoist, Focusmate, or Habitica offer ADHD specific support. Peer support groups can also be helpful when they align with your individual needs.

Final Thought

Receiving an ADHD diagnosis required me to rethink how this condition fits into my mental health story. Transitioning from a single diagnosis to a multi diagnosis life was overwhelming at times, but it also brought freedom.

The little girl who once shook her head to quiet the noise can rest now. I am in the driver’s seat. ADHD is part of my story, not the whole book.

Though there are more letters attached to my diagnosis profile, I am no longer afraid. I am informed, supported, and equipped with tools that align with how my mind actually works. There will always be challenges, noise, and unpredictability, but I face them with clarity, hope, and faith rather than fear.

To my readers:

What would shift for you if you stopped seeing ADHD as a failure to focus and started seeing it as a call to design a life that truly fits you?