Showing posts with label manic episodes. Show all posts
Showing posts with label manic episodes. Show all posts

Thursday, November 20, 2025

When the Battle Ends, Baseline Begins | My Jouney Back to Baseline - Part 5

 

When the Battle Ends, Baseline Begins

My Journey Back to Baseline Part 5

It has been a week since my follow-up appointment with Dr. A. Although I had convinced him to let me heal at home, I knew he had reservations about whether I could manage recovery on my own. He seemed pleasantly surprised when I walked into his office last week with Grama Judie by my side, calm and steady, ready to tell him I felt like myself again.

After a few questions about sleep hygiene and impulsivity, even he could see that his patient was on the mend. He told me how proud he was of my progress and recommended I stay on the new sleep medication a little longer until my circadian rhythm was stable. I agreed, admitting that sleep, more than impulsivity, had been my biggest challenge this time.

I was finally out of the woods. It had been a hard fought battle, but I was back to my baseline. For the first time in nearly twenty years of living with bipolar disorder, I felt like I was in control of my mental health, like I was in the driver's seat on my journey toward long term recovery.

Yet even when the battle ends and baseline begins, uncertainty lingers. Each episode, whether hypomania, mania, or psychosis, teaches me something new about who I am and what I am capable of. This most recent episode reminded me of my strength, resilience, and determination. I am a fighter. And with the support of my care team and family, I now know I can meet my mental health goals.

Choosing Healing on My Own Terms

It would have been easier to accept Dr. A's initial recommendation for hospitalization. But something in me knew I needed to try a different path. Healing at home was a risk, yes, but it was a risk worth taking for the sake of my autonomy, my future, and my dreams.

Since my diagnosis, I have often felt powerless, like I was living a life dictated by my illness rather than by choice. Every episode in the past left me feeling like I was slipping further away from myself. But this time, I fought to reclaim control. I chose to believe that recovery could look different, that healing could happen beyond hospital walls.

The Blessing of Baseline

Today, I carry a renewed sense of hope. The challenges that come with bipolar disorder, the highs, lows, impulsivity, and instability, are still part of my life, but they no longer define it. My approach has changed. I now face each cycle with wisdom, patience, and compassion. I have gained a deeper understanding of how this illness operates within me, and I am equipped with tools, structure, and support to face it head on.

I am not alone on this journey. My medical care team, my family, and my support network stand beside me, ready to help me weather whatever storms may come. When the next battle arrives, I will be ready, with faith, awareness, and the knowledge that every struggle brings growth.

Because with every battle comes a blessing, the blessing of baseline, the calm after the storm, and the start of something new.

Thursday, November 6, 2025

Recovery, Remission and Redemption | My Journey Back To Baseline - Part 4

 

Recovery, Remission and Redemption

My Journey Back To Baseline Part 4

I have learned a great deal in my two years of remission. I have continued outpatient treatment and I connect with Dr. A regularly for check-ins, medication management, and mental health emergencies. I built structure, routine, and healthy habits that support my emotional wellness. I have managed my medication collaboratively with Dr. A to ensure that I am on the therapeutic combination most likely to prevent bipolar relapse. I have been sober for almost two years, which has been one of the most important factors in stabilizing and protecting my baseline. I have also taken intentional steps to address trauma through psychotherapy. I am pursuing my passions through writing, blogging, and public speaking. I have secured stable housing with the help of my support team of family and friends.

For the first time since my Bipolar I disorder diagnosis in 2006, I was able to identify the trigger that set off this most recent hypomanic episode: excessive travel, exhaustion, and burnout. In the past, episodes escalated before I had any awareness. I would end up in the emergency room where the episode was often misdiagnosed as drug-induced psychosis. I would be admitted to the Psychiatric Intensive Care Unit (PICU) as an involuntary patient, experience isolation and restraints, and spend no less than two months hospitalized. I would be medicated heavily and discharged quickly, with little understanding of how to maintain my mental health outside the hospital or prevent the same cycle from happening again.

Fast forward to today. Through psychoeducation, trauma work, accountability, and deep self-awareness, I can now recognize triggers for both the highs and the lows of my mood disorder. I knew what was happening in my mind, and I sought help before the episode escalated into mania or psychosis. Over the last three years, I earned Dr. A’s respect through transparency and honesty in our appointments.

So when I arrived with an unconventional request to heal at home rather than in a clinical setting, he took a risk. He trusted my insight and believed in the work I had done to understand my illness. Dr. A has been more than a psychiatrist. He has acted as a collaborator in my healing. We do not always agree, but our relationship is grounded in mutual respect. That respect allows me to have agency over my mental health, something many people living with severe mental illness do not experience.

During the first week of healing at home, I felt like a newborn. My days consisted of showering, eating, sleeping, and sitting outside on my porch for sun and fresh air. I checked in with my support team, especially Grama Judie. I listened to audiobooks, colored, and played music to soothe the noise in my mind. When the doubt became too loud, I turned the music up and danced until I remembered that my body, too, could be a place of healing. I sang loudly, breathed deeply, and held space for myself in ways that were both simple and sacred.

Sleep did not come easy. I feared that at any moment this healing-at-home path could shift, leading me back into hospitalization. I was grateful, but I was also afraid that three weeks would pass and I would still be hypomanic. Mania felt close, like something waiting behind a door. Psychosis felt like a possibility. The medication could only carry me part of the way. The rest required trust, discipline, and faith.

I was not only chasing baseline. I was chasing redemption. If I could return to baseline on my own terms, I would regain my autonomy. I would show the people in my life that my illness did not define me or diminish me. I would show myself that I was capable of self-correction and emotional regulation. I would challenge the belief that hospitalization was the only path to stabilization.

If I returned to baseline with the support of my healthcare team, medication, structure, routine, healthy habits, my family, my friends, and my own relentless commitment to choosing myself each day, then maybe the question would change. Maybe I would not have to chase baseline anymore. Maybe I could begin chasing my dreams.

I would not receive the answer to that question until my follow-up appointment with Dr. A, where he would determine whether hospitalization was still necessary or whether I had found my way back to stability, remission, and the possibility of redemption.

Thursday, October 30, 2025

Recovery Challenges and Family Dynamics | My Journey Back to Baseline - Part 3

 

Recovery Challenges and Family Dynamics

My Journey Back to Baseline - Part 3

The weeks that followed my emergency appointment with Dr. A required patience, discipline, and a level of self-trust I had not fully practiced before. I began taking the new antipsychotic as prescribed, accepting that weight gain might be a side effect. I parked Betty White, my Toyota Camry, and committed to staying grounded. I replaced my 5 a.m. gym routine with quiet therapeutic walks. I slowed down. I focused on self-care. I practiced self-compassion, reminding myself that letting go of the rigid daily to-do lists was not failure but healing.

Staying out of "family business" was the most difficult term of my recovery. My mother was diagnosed with dementia in May 2024, and I became her primary caregiver. That role is not just practical but emotional. It means managing appointments, daily check-ins, and being her grounding presence. I also have two nieces who are used to having me close. My family loves me deeply, but even after twenty years of living with Bipolar I disorder, understanding the illness is not the same as living with it. The emotional toll of their worry has often pushed me to pretend I was okay before I was.

Dr. A made it clear that connection, concern, and caretaking could all serve as stress triggers during this stage. It was painful to accept that the people I love could also destabilize me. In the past, I rushed my recovery to reassure them that I was "back," placing their comfort above my wellness. This time, I chose differently. I chose to put my oxygen mask on first. I chose to heal at my own pace and in my own way.

Telling my family that I needed space was not easy. Some understood immediately and checked in gently through text. Others, guided by fear and memories of past episodes, urged me to go to the hospital and "let the doctors handle it." I knew I was taking the harder path. The unfamiliar path. The one that made everyone, including me, uncomfortable. I felt scared and hopeful at the same time. I felt relief.

And I was not alone.

My support team held steady. They believed in my ability to navigate this process at home. They saw my strength, resilience, and insight even on the days I struggled to see it myself. Their encouragement helped me stay grounded, stay committed, and stay open to healing.

The journey of a thousand miles begins with a single step. I finally believed I could take that step without surrendering to the idea that hospitalization was the only road back to stability. I began to rewrite what recovery could look like for me.

Not rushed.
Not reactive.
Not shaped by fear.
But steady, intentional, and mine.

Thursday, October 23, 2025

You Don’t Know What You Got Til It’s Gone | My Journey Back to Baseline - Part 2

You Don’t Know What You Got Til It’s Gone

My Journey Back to Baseline - Part 2

As I sat in the waiting room of Dr. A’s office at the hospital I once called home, I was terrified. To my right was the door to the inpatient unit, and I knew that after this difficult conversation, I might be returning there once again. Grama Judie sat to my left, quietly holding space beside me. I was in the midst of a hypomanic episode and I knew it, Grama Judie knew it, and soon my doctor would too. I sat in silence, rehearsing what I could possibly say to avoid being admitted behind the reinforced steel doors of the psychiatric unit I feared more than anything. When I looked up from my thoughts, Dr. A appeared, summoning us into his office.

My psychiatrist is a well-dressed, well-spoken Nigerian man who always seems in motion but somehow manages to slow down and give my care his full attention. We have worked together for almost three years, during which he has seen me in hypomania, mania, and psychosis. His decision to refer me to long-term care at a local psychiatric hospital once saved my life. It gave me the space to rebuild, rediscover hope, and find a healthier way to manage my bipolar disorder. If baseline represented recovery, this latest episode felt like relapse. I could only hope that my unconventional doctor would hear and support my unconventional idea for how to find my way back to baseline once again.

Dr. A began our appointment as he always does.

“What’s going on with you, Onika?”

That simple question broke me open.

“Doc, I’m having a hypomanic episode. I’m averaging one to two hours of sleep a night. My thoughts are racing. I spent my rent money impulsively. I’ve blown through my inheritance. I’m overwhelmed by family responsibilities. I’m hypersexual, though I haven’t acted on it. My appetite is gone. I have endless energy, and I can’t regulate my emotions. I keep crying without knowing why.”

I told him everything.

He listened, then spoke with honesty and care. He reminded me that he had warned me about overextending myself. The constant travel, the time zone changes, the lack of rest—all of it had pushed me past my limit. He had hoped I would slow down after my trip to Guyana last December, but instead, I took on more. A vacation in the Bahamas, followed by a 12-hour family road trip to New York City, then another flight soon after. He explained that for someone living with bipolar disorder, these disruptions can be dangerous. I had burned out my brain, and now it was no longer a question of if hypomania would escalate to mania, but when. His recommendation was voluntary hospitalization for two to three weeks to regulate my sleep.

In that moment, a lyric from Joni Mitchell’s Big Yellow Taxi came to mind: “You don’t know what you’ve got till it’s gone.” My baseline was gone, and with it, my freedom felt threatened. I knew what hospitalization meant. They would take my clothes, my jewelry, and my phone. I might end up in the Psychiatric Intensive Care Unit, where nurses could strap me to a bed or place me in isolation. I wouldn’t eat what or when I wanted. I couldn’t call my loved ones or return home when I wished. I would become a name on a whiteboard, a patient with no autonomy.

The weight of his recommendation hit me hard, and I made a decision in that moment: I was not going to be hospitalized. I believed there was another way to recover, another path to remission, and I was determined to prove it.

I made my pitch. I told Dr. A that being admitted to a psychiatric ward would set back my progress. The environment there was not conducive to healing. There was little trust, little communication, and too much control. I proposed an alternative, to heal at home. I promised to take the prescribed medications despite the side effects, to rest, to avoid driving, to reduce family involvement, and to listen to my body’s signals.

Healing on my own terms had helped me maintain stability for nearly two years, and I was desperate to try again. Something in my plea must have resonated because I noticed his expression soften. His eyes, behind his bright blue glasses, seemed to smile. Victory.

Dr. A agreed. He said I had shown great insight and accountability by coming to him before things worsened. He told me he was proud of my honesty and my commitment to wellness. Because our relationship was built on mutual trust, he would allow me to try recovery at home, under strict conditions: 

  • Take the new medications exactly as prescribed and prioritize sleep
  • No driving for three weeks
  • Skip the 5 a.m. gym workouts and stick to light walks in the neighbourhood
  • Complete all required blood work

  • Most importantly: stay out of family business

I left the office with Grama Judie by my side, clutching a new prescription and a fragile sense of relief. I had convinced my doctor to believe in me, to trust that I could find my way back to baseline outside hospital walls. His faith felt like a gift, and I was determined not to waste it.

As we walked toward my car, Grama turned to me and said with a grin, “If I think this isn’t working, I’m calling Dr. A and forming the hell out of you!”

I kissed her cheek, laughing through tears. My eighty-year-old grandmother, my advocate, my friend, and my fiercest protector had once again saved me from myself. Together, we walked toward my uncertain future, one built on hope, faith, and the belief that I could find my way home to baseline once again.

Thursday, October 16, 2025

Holding It All Together: Caregiving, Grief, and the Fight for Stability | My Journey Back to Baseline - Part 1

Holding It All Together: Caregiving, Grief, and the Fight for Stability

My Journey Back to Baseline - Part 1

My journey back to baseline has never felt harder than it has in recent weeks. Over the past 20 years of living with this complex and unpredictable illness, I have experienced countless hypomanic, manic, and psychotic episodes. I have been hospitalized for extended periods while doctors worked to guide me through cycles of mood swings, insomnia, and emotional instability. I have always known that psychosis lurks somewhere between my present and my future, an inevitable part of my bipolar cycle on the road to recovery.

But something has changed, or maybe I have. Since my last severe manic episode, which led to a four-month stay in a psychiatric hospital, I have learned that the journey back to baseline does not have to mean enduring chaos before finding peace. With the right support, determination, and self-awareness, healing can look and feel different.

The summer of 2025 was a whirlwind. I traveled, took on new projects, became a caregiver, and published three blogs a week so readers could walk beside me on this wellness journey. My adventures took me to both new and familiar places, but I failed to notice how exhausted I had become. I convinced myself that small adjustments to my sleep routine would keep me stable and moving forward. What I did not recognize was that my constant motion was not just ambition, it was avoidance. I was running far and fast, refusing to think about what I was really trying to escape.

In May 2024, my mother was diagnosed with dementia, and in the months since, it has progressed. Though she remains physically strong, her memory has begun to fade. Three other relatives in my family are also living with dementia, all at different stages of their journeys. It has been hard for us all because we are a close-knit family, bound by love and history. My Gran Gran Alvira used to say, “Family sticks together because when one of us bleeds, we all bleed.” Lately, I feel like I am hemorrhaging under the weight of my mother’s illness.

As the eldest daughter of two, I have taken on the role of her primary caregiver. My days are filled with doctor’s appointments, daily check-ins, travel companionship, financial management, and personal care. I needed to breathe, so I took a month off. But when I came home, the responsibilities were still waiting for me.

Then came another loss. In November 2024, I lost my sister-cousin to cancer. I have not allowed myself to truly grieve. The only time I let the pain in is during my weekly visits to the lakeshore, where we used to walk together. I go alone because I am afraid that if my family sees me fall apart, they will start whispering worries about my mental stability, predicting relapse before it happens. I know their fear is wrapped in love, but it does not help me process the hole that loss has left in my heart. I did not want to return to old patterns of coping with grief such as substance use or self-destructive behaviour, so instead, I ran again.

By the end of summer, it was time to face what I had been avoiding. My bipolar cycle had veered from my usual baseline into rapid cycling, swinging between highs and lows. By mid-September, sleep had become nearly impossible. I could not regulate my emotions. I was overspending, overworking, and overextending myself, trying to be everything to everyone: caregiver, student, daughter, granddaughter, auntie, listener, writer, and speaker.

It was time for an emergency visit to Dr. A, my psychiatrist.


Tuesday, December 17, 2024

A Bipolar Woman’s Self-Reflection on Fear - Part 2: Losing My Voice

A Bipolar Woman’s Self-Reflection on Fear - Part 2: Losing My Voice

I discovered the gift of my voice, my ability to express myself through sound at 1-years-old. Honestly, I haven’t stopped talking since other than taking a moment here and there to reflect. If you ask my father, he will say I loved the sound of my own voice. If you asked my teachers, they would say I was an excellent student, but I talked a little too much in class. If you ask me, I just think I have a lot to say so the spoken word comes naturally to me.

 

But shortly after I turned 33-years-old I lost my voice. And I’m not talking about losing your voice because you have a sore throat. For three days this past January 2016, I lost the ability to speak and no one could explain why. I got up one morning and I felt physically weak, disoriented and dizzy. I lived alone so I had no opportunity to say a word until I left for work. I remember taking an Uber in because I felt so unbalanced I could barely stand. When the driver said ‘good morning’ I attempted to reply, and the words came out slow and slurred.

I immediately called my mother and when I couldn’t reach her, I called my Grama Judie. I told her my symptoms and she said I should head to the hospital. For many reasons I dislike hospitals and refused to go, instead choosing the nearest walk-in clinic. I was barely in the door before I lost consciousness and collapsed. I was taken into one of the exam rooms and the nurse had called an ambulance. She was trying to keep me alert by asking questions, questions that I tried to answer but I couldn’t. I was confused and terrified because when I opened my mouth the answers I formulated in my head just wouldn’t come out.

 

The ambulance arrived and transferred me to St Michael’s Hospital in Toronto. By the time I arrived at the emergency room I had managed to give them basic information about myself as well as my phone to contact my mother. The doctors ran every test they could think of, they feared I may have had a stress induced stroke. The MRI, EKG and blood work came back normal. Because I disclosed my history of mental illness, the next step was a psychiatric evaluation. This was what I had been dreading.

It has been my experience that when a person suffers with mental illness, doctors tend to overlook physical symptoms and label the problem a psychological one then pass you off to the ER’s Psychiatric Crisis Team for assessment. I was terrified of being admitted to the psychiatric unit. I knew that the likelihood was this was a reaction to a new antidepressant I was taking but to admit that would be to risk getting admitted. Though it was a struggle I managed to make my wishes clear: There’s something physically wrong, I am not crazy, I do not feel like harming myself or others and I want to go home.

After asking me a series of questions that I was all too used to answering, the ER psychiatrist advised that she feared this may be psychosomatic but not something to be admitted over. My mother finally arrived, and the doctors cleared me to go home and have her monitor me for the next few days. The relief I felt was overwhelming.

During those three days of silence, I really started to question how I had gotten to this point. Maybe there was another reason, hidden deep inside myself that I was failing to examine. Since the new year started, I have been taking on more, pushing myself harder mentally, physically and emotionally. I was beginning to feel pressure at work, I was lacking in sleep, my appetite was non-existent, and I was running from the depression that historically took over my mind every Winter since I was 17-years-old.


I was doing too much, and I was wrestling with the darkest parts of myself. I was overwhelmed and I knew it had everything to do with my mental health challenges. I was tired of running from it, I was tired of keeping the secret of my mental disability from my friends, colleagues and anyone I had any significant connection with. It was like a gaping sore that refused to heal, that was a constant source of pain as if trying to tell me: Until you deal with me, I am not going anywhere.

I had been thinking about telling my story, telling the truth for a while and during this experience my mind was in a constant state of remembering. Remembering the dark reality of my past, retracing my steps to see where I could have changed things, worrying that once the carefully constructed mask that I had relied on for so long was crumbling in the face of this truth. Even though my voice was lost, my thoughts were finding their way to the surface. All the lies I had told to protect myself, all the things that I could only remember pieces of from all the times I lost my mind to the overwhelming sense of failure I felt every day since I was a child. I knew it was time to face all that I had done, all that I had been through. My body’s betrayal at this critical juncture of my life was telling me that if I were truly going to move forward, I had to speak my truth.

I was ready and I was not ready. I was certain and I was not certain. I was terrified and calm because I knew it was time for the words to come out. I knew if my voice returned, I had to use it to tell the story of a woman who was abused in so many ways; a woman who lost her mind so many times only to find it again; a woman who has done things she was ashamed of; a woman who survived when the odds were stacked against her.


I knew my story could help people like me see that it is possible to go through things, terrible, life-changing, dark and destructive things and still come out on the other side fighting and hopeful and determined to achieve the impossible. To come through everything while still having faith that the next step, the next journey, the next dream will be the right one, the better one, the one that will finally make you whole.

It is possible to believe that you can survive your pain, only suffering as long as it takes you to learn your lessons. Then you take that newfound knowledge and change your life into something authentic. I want to be a force for this kind of change in people’s lives, giving them hope that happiness lies beyond the darkest waters.

I have always known this was my purpose, but I hid my light for reasons that seemed far away and inconsequential in the face of losing my voice. It was a new kind of pain to think that I had wasted so many years hiding from the world, hiding from myself that now, when I was on the precipice of taking my place and serving my purpose, there was this new obstacle that I was not sure I could overcome.


If all the world’s a stage like Shakespeare once wrote, then those three voiceless days were my version of stage fright. I learned that as much as I was afraid of the truth, if I continued to hold it in, I was in danger of losing the opportunity all together. The labour of having to force out every word, syllable by syllable, at a snail’s pace as if I had never spoken before was eye-opening.

I thought to myself, “What now Onika? You have all these words locked inside your mind, you have hoarded all your experiences, all that knowledge and wisdom never really sharing it with anyone and now you have finally found some courage to speak your truth, and you have lost your voice…you have lost your way.” When my voice did return slowly over the following days, the relief I felt was palpable. It was like being given a second chance to start my purpose-filled, passion-filled journey.


It’s time to embrace something that has always been difficult for me—change. I need to be fearless and learn to embrace change like a warm hug instead of running from the danger of the unknown. I have to embrace the journey I am on and pray to God that He will be there to catch me if I fall again and to keep me grounded when I finally rise.


Final Thought


In 2016 fear had a strangle hold on me. I was living a lie believing that if I told the truth about my Bipolar diagnosis to my new employer, colleagues and friends I feared rejection, I feared isolation and I feared I would lose my job. I believed my disability was a deficit and a detriment to the new life I was trying to build in a new city. After years of manic episodes, depressive episodes and hospitalizations I convinced myself running from the truth of my circumstances was the only way. I thought reinventing myself based on a lie would keep me safe and would lead to my ultimate success. 


But the opposite occurred, all the lying and deception and running away from my truth took a mental, spiritual and ultimately physical toll on my body. It was my mama that taught me the lesson “Speak the truth and speak it always cost it what it may.” and in 2016 not telling the truth about a significant part of my life cost me my voice. I became lost in a lie and I remember bargaining with God that if I got my voice back I would use it to share the truth about my lived experience with Bipolar disorder, the good, the bad and all the ugly bits in between. That experience taught me how dangerous fear can really be and I am so grateful my temporary paralysis lifted and I’m presently living in the light of my truth. 


A Bipolar Woman’s Self-Reflection on Fear is a series of entries that will allow you a window into my past and insight on my present and the lessons I’ve learned over the years that have put fear in my rearview mirror. 


Coming Soon

I have also decided to share with you the lessons that inspired me to be fearless and relentless in my pursuit of happiness and success. I will be posting the life lessons that have shaped and influenced my personal growth and development. A Bipolar Woman’s Self-Reflection: 42 Years of Lessons series begins on December 30, 2024, my 42nd Birthday. It is my hope that these lessons will touch your lives and inspire positive change on your journey to wellness. 

Monday, November 11, 2024

My First Manic Episode: A Woman’s Perspective on Bipolar Disorder

My First Manic Episode: A Woman's Perspective on Bipolar Disorder

“I didn’t see it coming until it was here.” This sentiment resonates deeply with anyone who has experienced a manic episode, especially from a woman’s perspective on Bipolar disorder. The whirlwind of emotions and thoughts can leave you reeling, and before you know it, you’re in the midst of something far beyond your control.

In this post, I aim to share my journey, illustrating the extremes of a manic episode and the profound effects it had on my life. My hope is that by sharing my story, others might find understanding, connection, and perhaps the courage to seek help.

Understanding Manic Episodes

A manic episode can be described as an extreme and uncontrollable elevation of mood, often accompanied by feelings of excitement or euphoria. For me, the initial surge of energy felt like a spark igniting a fire. I was flooded with ideas, racing thoughts, and an inflated sense of self-esteem. I felt invincible, believing I could accomplish anything. However, as thrilling as it was, I was unaware of the shadows lurking just beneath the surface.

The symptoms of mania are multifaceted. They can manifest as:

  • Rapid speech: I found myself talking a mile a minute, unable to slow down or catch my breath.

  • Disorganized thoughts: My mind raced, bouncing from one idea to another, making it nearly impossible to focus on anything.

  • Delusions of grandeur: I believed I had extraordinary abilities and a purpose that I was destined to fulfill.

  • Impulsivity: Financial decisions became reckless, and relationships strained under my new-found bravado.

  • Paranoia: I felt as though everyone was watching me, judging my every move.

As my episode progressed, these symptoms intensified, leading to hallucinations and even violent outbursts. It’s a stark reminder that, if left untreated, Mania can escalate into Manic-psychosis, where the boundaries of reality blur dangerously.

Men vs. Women: A Distinct Divide

Research shows that the onset of Mania typically occurs earlier for men, often in adolescence or around 4-5 years before women. Men may experience more intense and frequent manic episodes, while women often grapple with depressive episodes more frequently. For men, aggressive behaviors can surface during Mania, whereas women may experience rapid-cycling or seasonal episodes, leading to a different emotional landscape.

For me, this gendered experience of Bipolar disorder added layers to my understanding of my condition. I often felt caught between the heightened emotions of Mania and the stark reality of Depression, wondering how my experience compared to that of my male counterparts. After experiencing 13 episodes in my lifetime I can classify my Mania as rapid-cycling or seasonal episodes followed directly by severe depressive episodes.

The Triggering Events: A Perfect Storm

My manic episode was precipitated by a series of stressors that I couldn’t have anticipated. On my 22nd birthday, my grandmother passed away, a loss that shattered my emotional foundation. Just eight months later, I lost my other grandmother, compounding my grief and leaving me feeling adrift.

In an attempt to cope, I turned to substances like marijuana, seeking relief from the overwhelming sorrow. But rather than finding solace, I only intensified the storm brewing inside me. I struggled to focus on my final year in university, plagued by insomnia and a deteriorating relationship with my then-boyfriend. It was a perfect storm of emotional upheaval and loss that I didn’t see coming.

What the Episode Looked Like

As I spiraled into my first manic episode, I experienced a barrage of symptoms that became increasingly difficult to manage. Rapid speech turned into disorganized thoughts, and my once coherent conversations devolved into chaotic rants filled with delusions of grandeur. I believed I could change the world, that I had a mission that no one else could comprehend.

In the throes of Mania, my emotions felt like a pendulum swinging wildly. I laughed uncontrollably one moment, only to erupt into tears or anger the next. I remember feeling detached from reality, caught in a dissociative state where nothing felt tangible or grounded. My parents, concerned for my well-being, noticed the drastic changes in my behavior and knew they needed to intervene.

How My Parents Got Involved

My mother was just five minutes away from leaving for her 12-hour nursing shift when my boyfriend at the time reached out to her, desperately conveying how out of control I had become. That call prompted a frantic drive of four hours to Ottawa, where I was living at the time. I was hallucinating, lost in a world that felt all too real yet completely fabricated.

During the drive home, I tried several times to jump out of the moving vehicle, a clear indication of my disorientation and desperation. My mother, a nurse, assessed the gravity of the situation and recognized that I was experiencing a serious psychotic episode. She made the decision to take me to Scarborough General Hospital for psychiatric treatment.

The Hospital Experience

Arriving at the hospital was surreal. I was so far removed from reality that I couldn’t comprehend the seriousness of my condition. The staff deemed me a danger to myself and others, and I was restrained to a bed to prevent any further outbursts or attempts to escape. It was a terrifying experience to be chained to a bed, sedated into a haze of confusion due to the intense psychosis and my prolonged lack of sleep—I hadn’t slept for 52 hours.

When I finally regained consciousness, I found myself in an isolation room, disoriented and frightened. It was here that a psychiatrist diagnosed me with Bipolar I disorder, attributing my episode to substance use. He explained that I was essentially allergic to marijuana, and its use had triggered this manic episode.

Post-Episode: The Depths of Depression

After my manic episode, the reality of Bipolar disorder set in. I faced an extreme and prolonged Depression that left me feeling hollow and isolated. Sleep became my only refuge, and I would often stay in bed for hours, neglecting personal hygiene and losing interest in everything I once loved. I experienced a significant loss of appetite, leading to dramatic weight changes as I transitioned from manic energy to profound lethargy.

Social activities became daunting, and I withdrew from friends and family, fearing their judgment. Suicidal ideations crept in, an ever-present reminder of the darkness that enveloped me. This cycle of Mania followed by crushing Depression left me grappling with the reality of my condition.

The Stigma of Support

Navigating the stigma surrounding mental health proved to be one of the most challenging aspects of my experience. While I knew I was sick and needed help, the thought of entering the mental health system filled me with dread. I didn’t want to be labeled as someone with a mental disability, fearing the societal repercussions.

In the job market, having a mental health condition can feel like a scarlet letter, making it harder to find employment. Insurance applications often discriminate against those with invisible disabilities. When I was well, I felt invisible; but when I became unwell, it was as if my struggles were on display for all to see.

Many people choose to suffer in silence rather than risk the vulnerability that comes with seeking help. The fear of being treated as a second-class citizen in society can be paralyzing, and it often leads individuals to avoid the support they desperately need.

Managing Symptoms and Stressors

I learned that managing my symptoms equated to managing my stress. Self-awareness became crucial; I had to recognize what stressed me out and have the courage to walk away from toxic relationships or situations, whether they involved family, friendships, or even jobs.

I took small steps toward understanding my triggers and incorporating healthy coping mechanisms. Mindfulness practices, journaling, and regular exercise helped ground me. Surrounding myself with understanding friends who offered support without judgment was essential in my journey toward stability.

The Journey Toward Acceptance

Over time, I learned to accept my condition as part of my identity, rather than allowing it to define me. Seeking therapy and engaging in medication management became vital components of my routine. I learned to communicate openly with my loved ones about my struggles and sought to educate them about my condition.

Embracing my journey and sharing my experiences became therapeutic. I realized that breaking the stigma surrounding mental health starts with conversation. I found strength in vulnerability, and it empowered me to advocate for myself and others navigating similar paths.

Final Thoughts

Reflecting on my first manic episode, I realize it was a wake-up call—a moment that reshaped my understanding of myself and my mental health. The experience was both harrowing and enlightening, revealing the importance of community, understanding, and acceptance.

If you find yourself grappling with similar experiences, remember that you are not alone. It takes courage to seek help, to share your story, and to confront the stigma surrounding mental health. Together, we can foster a community of support and understanding, ensuring that no one has to navigate these turbulent waters alone.

For those looking for more resources, be sure to check out my post, How to Start Managing Bipolar Disorder: A Comprehensive Guide, for tips and strategies. Let’s continue to have conversations that take us beyond the stigma, share our stories, and support each other in this journey toward healing and understanding.