For years, I treated every difficult feeling like a bill I had to apologise for immediately. A headache, a racing chest, the low fog that followed me through a shop: I would say, “Sorry, it’s nothing,” before anyone could ask a follow-up question. I had learned that needing care was acceptable only if I could make it small, efficient and mildly entertaining. Even my anxiety was supposed to arrive with a joke attached.
One afternoon, a friend asked how I was, and I answered, “I’m not okay.” Then I apologised for the answer. She did not tell me to brighten up or offer a suspiciously neat solution. She said, “Okay. Do you want company, distraction, or help finding support?” That small question gave my distress a shape I could hold without defending. It was the beginning of learning to speak plainly, though the old reflex took months to loosen.
The apology came from somewhere. As a child, I was rewarded for being easy, for noticing other people’s needs and treating my own as inconvenient. As a bisexual woman, I also grew up around the idea that taking up space required a defence, especially when my body, identity or emotions did not fit a convenient story. Feminism taught me that everyone deserves authority over their own life; I had not yet applied that authority to my own panic.
In Sydney, Melbourne and Brisbane, the polite language of getting through a day can sound deceptively small. On a crowded train, in a shared office kitchen or during an endless stand-up meeting, “sorry” and “no worries” smooth over friction. I knew that script well. I apologised for taking a sick day, for asking a clear question, for needing a bathroom break. The apology made me feel considerate while quietly convincing me that my needs were an imposition.
I began to separate two kinds of responsibility. If I made a mistake that affected someone else, an apology could repair harm. But I did not owe anyone an apology for having a body, having a mental health condition or having a limit. “I’m sorry I’m struggling” asked the listener to forgive my existence. “I’m struggling, and I need support” gave them information they could choose to respond to. The second sentence was not less polite. It was simply more honest.
Learning was not a single brave confession. It was therapy, awkward phone calls and several attempts to explain a panic attack to a manager. My therapist helped me notice the difference between describing a feeling and apologising for it. We practised short sentences, because in the middle of anxiety, a long explanation felt impossible. I also learned that asking for support does not require me to prove I have reached the worst possible outcome.
I started replacing the automatic apology with a clear request. At first I said, “I’m having a rough morning,” and then I added, “Could we move the meeting?” Later, I could tell a friend, “I’m not safe with this thought alone; can you stay on the phone while I get through it?” Nothing about that sentence was dramatic. It simply located the problem and invited a specific kind of care. Precision felt kinder than pretending everything was fine.
That shift changed my relationships as much as my calendar. I had spent years managing other people’s feelings so that I would not be difficult to love. Naming distress meant accepting that closeness includes room for a bad day, a cancellation or a different kind of conversation. It also meant rejecting the idea that women, queer people and caregivers must always be the emergency contact for everyone else. I could be a friend, a sister, a worker and a person having a difficult month, all at once.
Finding practical help was easier when I stopped treating the first appointment as a performance. In Australia, a GP can assess mental-health needs and create a Mental Health Treatment Plan, which can open access to Medicare-subsidised psychological sessions. Bulk-billing and telehealth have made appointments possible for people who cannot easily take time off work, although availability still varies sharply between suburbs and cities. When I called a clinic, I did not need a diagnosis. I said, “I’m not coping, and I want support.” The receptionist asked when I was available, and the conversation became ordinary.
Confidentiality mattered, so I checked the rules rather than relying on vague promises. The Australian Privacy Act 1988 and state and territory privacy laws generally protect health information; state mental-health legislation also sets rules around assessment and involuntary treatment. Mandatory-reporting and serious-imminent-danger exceptions are real, and they vary by jurisdiction. Knowing the limits did not make me less entitled to privacy. It made me more informed about what I was agreeing to and who could see my notes.
Having information did not mean I had to use it immediately. I kept the numbers somewhere easy: 000 for immediate danger, Lifeline on 13 11 14, and the Suicide Call Back Service on 1300 659 467 for a structured support call. Knowing there was a human voice available made the gap between crisis and action feel smaller.
I also learned that public systems have gaps. The NDIS can fund supports for eligible people with psychosocial disability, but it is not a general anxiety program, and waiting lists can be agonising. A GP referral, a private psychologist and an NDIS plan are not interchangeable. I found asking for help while looking for a way to describe the first step without turning it into another performance. The page was useful not because it promised an easy route, but because it reminded me that asking could be modest, practical and free of performance.
I keep a few practical tools in my phone’s Notes app, ready for the moment my brain goes blank. These ways of speaking are not meant to convince anybody that I am fine. They make the truth usable by explaining what is happening, what I need and what happens next.
These sentences fit ordinary Australian days: a kitchen catch-up after work, a message to a team group, a call made while standing outside a Coles or Woolworths while a groceries order changes in the app. They do not require a dramatic story. A flat white or long black and a quiet five-minute walk might be part of my care plan, but a coffee cannot do the work of therapy, sleep or safe housing. Naming what is missing is how support becomes specific.
Most importantly, I can use these phrases without attaching a second speech about how inconvenient they are. I can say, “I need to reschedule,” and stop. I can decline an extra shift without apologising for being tired. Knowing my rights under Australian employment and workplace health-and-safety rules does not mean I must disclose a diagnosis. For some adjustments, I can describe what I need without sharing a diagnosis. Honesty can have boundaries.
These days, I say “I’m not okay” less like a confession and more like a signal. Sometimes the signal is quiet: I cancel a plan, text a friend or sit in the car until my breathing settles. Other times it is loud enough that I ask someone to stay. I no longer treat calmness as proof that I am recovered, and I no longer confuse a hard day with a failed life. Recovery has become a practice of returning, not a performance of being fine.
I also keep the lesson connected to the world beyond my own story. Personal wellbeing is not separate from the conditions that make exhaustion, shame and fear so common. I read site updates when I need reminding that individual care sits alongside community action, and I try to make room for other people’s “I’m not okay” without demanding that they educate me. The point is not to turn every confession into a campaign. It is to refuse the demand that vulnerable people make themselves harmless first.
The work is still personal, which is why I keep one concrete promise to myself. Tomorrow morning, I will call my GP and ask to review my Mental Health Treatment Plan.