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.


Monday, September 29, 2025

One Year of Onika L. Dainty: Over 43,000 Views, Real Stories, Real Growth

 

One Year of Onika L. Dainty: Over 43,000 Views, Real Stories, Real Growth

The Post I’ve Dreamed of Writing

One year ago, I pressed publish on my first blog post with a mix of fear and hope. Today, I sit here in awe: over 43,000 views in 12 months. That number represents more than traffic. It means reach, resonance, and community.

This space was never about numbers, it was about honesty, about putting lived experience with bipolar disorder on the page and trusting that someone, somewhere, might feel less alone. Along the way, I’ve written through highs, lows, and all the in-between spaces of recovery.

The Personal Wins: Living the Dream of Writing

For years, I dreamed of being a writer. This blog made that dream real. Weekly practice gave me courage to tell the truth, even when it felt risky. Vulnerability became a ritual, not a performance, and self-trust slowly replaced self-doubt.

Every time I published, even on the toughest days, I met a truer version of myself. And in doing so, I also get to lead by example, showing my two nieces that you can follow your dreams, even when the path is complicated by mental health struggles.

Readers’ Favourites: The Posts That Traveled Farthest

Some pieces traveled farther than I ever imagined:

  • Life Lessons Series - This ongoing series of reflections has become a hub of dialogue. Posts on validation, resilience, and self-love showed me that sharing “small” lessons can carry immense weight.

Together, these four pillars helped carry us to nearly 43K+ views—proof that honest, grounded stories matter.

The Professional Wins: From Blog to Real-World Impact

This blog also opened doors beyond the screen.
  • Speaking engagements: I’ll never forget the first time I stood on stage and saw people leaning in to hear lived experience framed as knowledge.
  • Course development: Partnering with a university to help shape curriculum affirmed the value of storytelling and empowered the next generation of social workers.
  • My own course (coming soon): A space where lived experience meets structured learning for women navigating mental health recovery.
  • Peer support at scale: From DMs to workshops, the ripple effect of one blog post has reached further than I could have imagined.

The Honest Lows: What Was Hard and How I Coped

It wasn’t all triumph. Creating while living with bipolar disorder meant navigating cycles, hospitalizations, and travel that disrupted consistency. Family duties and responsibilities demanded renegotiated boundaries. And sometimes, I had to pause projects or choose rest, learning that stepping back is also part of moving forward. 

You may have noticed that this past month, September, and also in May, my posts were limited. That is because I have been moving through bipolar depression and hypomania, and I chose care over output. I will share more about this in future posts.

My Support Team

I have often spoken about the importance of having a team around you, and mine has been incredible. A special thank you to Grama Judie for everything she has done for me, for being my advocate when I cannot be my own. And to my family, who have been on this journey with me and stayed by my side, you know who you are.

Sidebar: My Relief Kit

  • Journaling for grounding
  • Walks in nature
  • Music playlists for mood shifts
  • Phone calls with trusted supports
  • Sleep hygiene rituals

What I Learned About Myself in 365 Days

  1. I am both tender and capable.
  2. Vulnerability is a practice, not a personality.
  3. Consistency comes from systems and support, not willpower alone.
  4. My path is mine to honour, to pace gently, and to protect fiercely.
  5. Community multiplies courage.

What’s Next

The second year brings new commitments and possibilities:
  • More consistent blogging with a sustainable cadence.
  • Partnerships with local organizations and peer networks.
  • Exploring a not-for-profit initiative to support those navigating housing, mental health, and women’s wellness.
  • Courses and workshops that translate lived experience into structured tools for healing and resilience.

Gratitude Roll

To every reader, commenter, collaborator, and quiet supporter: thank you. Thank you for trusting me with your stories, and for letting my words walk alongside yours.

I’d love to hear from you: Which post spoke to you most? Explore my previous posts and the Life Lessons Series and let me know.

If a post has helped you, please share it with someone who needs lived-experience hope today. Together, we can keep this community growing.