Diagnosed with Tourette’s Syndrome, 11-year-old Tryxx Maysey can’t control their hidden disability.

I’m not a naughty kid. You might think that I am being controlled by some sort of demon or that I’m off with the pixies in fairy land. That’s simply not true: I am suffering with a hidden (or not- so-hidden) disability, a syndrome that only one in a hundred Australian kids live with.  

Tourette’s Syndrome (or TS for short) is a neurological disorder that I can’t control. It causes my body to do movements or make sounds on its own accord, called tic-ing. This might be putting up the middle finger or using swear words. But this doesn’t mean that I’m a naughty kid; it’s my TS that makes me act in the way that I do. 

Being 11 years old and in my final year of primary school, I am moving closer to the next step of my school journey. While at times I have felt like a classroom distraction, my friends and classmates over the past few years have been very kind and supportive of me and my Tourette’s.

There are some respectful and kind teachers too, who have taken the time to understand my condition and to offer the best help they can. Many of my classrooms offer a “safe zone” right behind the teachers’ desk where I can go if I start to feel overwhelmed, and when I am feeling overstimulated by noises, I have some noise-cancelling headphones which can also play music! 

Isolated and misunderstood

Yet at times, it feels as though the kids at school get it better than the grown-ups. Over the years, some teachers’ negative and nasty words and reactions have left me feeling scared, isolated and misunderstood. Many times, my friends have had to stand up for me against a teacher when my Tourette’s has left me in a petrified state. 

Hearing the word stop is nothing new to me: It is something I hear quite often from those who do not understand how Tourette’s can make me act.

For example, when I went kayaking for a school excursion with some friends, we were told by the activity leader not to shake our kayaks otherwise they’d tip over. But to someone with TS, telling them what not to do is almost like a green light for their tics to start doing that very thing—our minds are mean to us like that.

So of course, my tics started, and I began to shake my kayak. One teacher aide yelled at me, telling me over and over to “just stop”. No matter how hard I tried to explain myself, they simply could not understand that it is impossible to control my tics. Yet, if I were in a wheelchair, they would not expect me to “just stand up”, and I’m sure they wouldn’t tell a mute person to “just speak up”. So why is it any different for me?

Finding success in school

Regardless of my disability, I can be successful just like the rest of my classmates who aren’t affected in the same way I am. At school, I am within the top 10 per cent in academics, and I am also a school leader. Still, statistics show that close to half of all people with TS report that they’ve been told off by a teacher, and a third have reported being kicked out of a school classroom. 

Going into high school, I am starting to feel anxious. Many of the people I have met so far have been very kind, but there is still unawareness, fear and frustration.

Recently, I attended a high school open day and I began to tic while watching an important presentation, and the school staff were admittedly unprepared. However, it’s not difficult to make considerations if you know what to do. 

With two-thirds (63 per cent) of people in the TS community feeling that their teachers and teacher aides haven’t been trained properly to deal with Tourette’s, something needs to be done. Most of us—in fact, 88 per cent—believe that the government should be doing more to train teachers.

I often feel nervous to tell my teachers that I have Tourette’s, especially due to the stigma around the disorder. Many forget to take the time to understand the person, to get to know the person and to see the person, not the disability. 

What you see when I am tic-ing is not who I truly am. I am not a naughty kid.

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