It took me ten years to get officially diagnosed with Generalised Anxiety Disorder – a mental illness I knew I had the moment I heard about in my post-secondary Psychology class. There was a wave of clarity that swept over as I felt my eye twitching again. That day, I had to hold back tears during the lesson, because a part of me knew how hard it was going to be to get anyone to believe me.
I knew that taking on this label would come with its own challenges – mainly on how I was perceived.
I had to see my own mother go through the same thing when she was given her first diagnosis, and then her current one a few years later. The way that our family dynamics changed so drastically – because whilst my mother was struggling, the belief in her ability to recover and maintain herself was so fragile.
My mother became associated with her worst days – days when she couldn’t leave her bed, days when she lashed out or punished herself.
At one point, it became so glaring that even she couldn’t see herself outside of her illness, outside of her suffering. So how could she accept anything else?
Taking all of this in, at only 16, I still asked to go to therapy. I remember feeling my stomach drop when they asked me why, that I seemed okay. I wasn’t “that bad” (but really I was just very high-functioning). But I kept pressing, kept asking, and eventually, I got into that room.
It helped when I went, but life happened – there were times when I couldn’t afford to go because I had to prioritise other needs. My parents, at first, didn’t want to help. Eventually, they agreed.

But even then, talking therapy wasn’t enough. It wasn’t until I was 25 that the idea of medication came up with my therapist. I remember the tears I shed to my therapist, explaining how I could no longer tell what my reality was because I couldn’t sleep or eat.
How I cried again at my family doctor’s appointment, and supplemented the request of medication with a two-page document of all of my symptoms. That day was a Thursday in April, and I remember the absolute relief that I felt once the medication was in my hand.
But with this label came a perception issue. When people hear “mental illness”, “depression”, “anxiety”, they think of specific images and experiences. Irrationality, chaos, unpredictability – all things that can’t be easily understood.
So, no matter what I did and how well I did them; when there were issues that led to me needing to voice my feelings and anxiety, that was all they could see. I was no longer an asset or a stable presence – I was confusing, a liability. My ability to “function” was overridden by my label as a mentally ill person.
But, like my mother, I am more than my diagnosis; I am more than my bad days and moments – and our labels don’t exist to restrict us, but to help us and the people around us understand our lived experiences.
Bad days will happen, but less than good ones. Some days, we will be hard to understand. But what sets our loved ones apart are those who meet us with compassion and empathy, rather than judgement and prejudice.









