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Artist of the Month

Since 2023, we have been making it our mission to highlight a new artist from the Australian theatre scene each month.

This individual could be a performer, director, writer, reviewer, sound designer, musician, lighting designer, set designer, stage manager and so on.

If you feel like you’d know someone who would be perfect, contact us or hit us up on our socials @theatrethoughtsaus.

December - Brittany Goh

Musical Theatre Performer & Disability Activist

Brittany Goh is a 19-year-old performer, content creator and aspiring disability advocate living on unceded Gadigal Land. After moving to Australia from Aotearoa, New Zealand, she began training in singing, acting and dance, hoping to bring visibility to disabled performers in the Musical Theatre industry. Since moving to Sydney, she performed as Beth March (Alternate) in Little Women (Company of Dramatic Arts).
 
Most recently, Brittany was accepted into the NIDA Diploma of Musical Theatre (Class of 2026), making her the first wheelchair user to be accepted into the program to study, and the first wheelchair user to begin studying a tertiary Musical Theatre program in the country. Brittany was also offered a place at Brent Street’s Diploma of Musical Theatre.
 
As an autistic wheelchair user, Brittany strives to use her platform on social media to give hope to other aspiring disabled performers and raise awareness and understanding about disability, both in and out of the performing arts.

My Story

What inspired you to get involved in theatre?

When I was a kid, I saw a production of Phantom of The Opera in Auckland. It was in 2016, so I must’ve been 9 or 10 years old and at the time my entire personality was My Little Pony so I didn’t expect to enjoy it, but by ‘The Final Lair’, I was crying. There was something magical about it. People performing live, telling stories and the way they did it through song and dance, and – for some reason – it was something I really connected to. That was rare for me. I hardly ever connected to anything growing up, people or things, but the inexplicable times that I did, that connection was strong and I’d engage every minute of my time in it. I left the theatre knowing that performing was something I wanted to be a part of, and my parents enrolled me in singing lessons not long after.
 

Do you remember the moment you wanted to do this as a career?

Watching Phantom Of The Opera was definitely when I decided I first wanted to do this as a career, but also I do remember the moment I decided to pursue this as a career. In February of 2025, I saw a competition for front row tickets for the opening of SIX in Auckland and a meet and greet with the queens (and Lucy Moss!). I loved the musical, and I can’t say no to free tickets, so I entered a video of myself singing ‘Heart Of Stone’ and I managed to win! 
 
Like when I saw Phantom as a kid, I was hooked. I saw SIX four times total, made a custom funko pop of Katherine Howard, looped the soundtrack on repeat, even made an entire Katherine Howard costume that I had designed and adapted to be suitable in my wheelchair! Not long after the last time I saw the show, I received an email advising me to leave the institution in Auckland where I was enrolled at to study a bridging course towards Medical Imaging and that it was not an accessible career path. 
 
I was relieved. The entire time I was dreading having to study it, and even before I’d even received that email, I was looking longingly at courses in Musical Theatre. So, I called up my parents later on the night I got the email and told them I wanted to try auditioning for tertiary programs for musical theatre in Australia. I couldn’t spend the rest of my life regretting not pursuing it, and if I was always going to deal with inaccessibility everywhere and my disabilities would always make my life harder, I might as well do something I loved so that the fight was worth it. 
 
What do you see as your ‘voice’ in the industry, as it stands?
 
There aren’t many people in musical theatre who are visibly disabled or vocal about their disabilities. Even though there are a lot of neurodiverse and invisibly disabled performers, there’s a lot of stigma and shame around illness in theatre; it affects non-disabled people too. But I can’t hide my wheelchair, or my disabilities, and I also don’t want to.
 
I strive to tell my story and the stories of other disabled people, of all of the people who have messaged me on social media and commented on my posts who have been pushed out of theatre because of inaccessibility, of the ones who can’t perform anymore because they’re too sick, the ones who feel like it’s impossible or they’re alone and don’t have a voice or community. It’s important for me to make people feel seen, to inspire and give hope to the people like me and prove to them it’s not impossible — I wish I had that when I was younger, to feel like even if I did become disabled, it was possible.
 
But in that, I also feel a responsibility to be vocal about the struggles I face with disability and/or chronic illness, the ones that are inherent to having a condition, but also the external ones of ableism and inaccessibility. Disabled people deserve to feel seen, to find community and representation in the good and the bad. They should get to see people achieve, not because they don’t struggle, but because there is a community of people cheering you on, spaces that want to accommodate you, teachers and castmates and loved ones that care, that will do what it takes to have you there and learn and understand because they value you and your perspective. That all makes it a little less hard.
 
I also try to educate people outside of our community about the things we face, to help build understanding and connections with non-disabled people and performers, because while we share the same dreams, it’s a much different journey to get there, but in the end we’re all here because we love the art of theatre. But my voice isn’t just the loudness or the vocal activism, it’s things like just showing up, choosing not to apologise or make myself small in my wheelchair, wearing my headphones and sunglasses and earplugs when I need them, bringing Theodore The Frog (my comfort item) when he’s needed. It normalizes disability and differences to people. It’s casual, and that’s important too. 

Where do you see yourself going/want to go next?

I guess I don’t really see myself going any one particular place. I used to make detailed plans as a kid, but it really messed with me when I realised I’d probably never accomplish the things I wanted to in the way I imagined. Nowadays, I just focus on one bigger goal that’s definitely achievable — for me, that’s been my promise that I wouldn’t give up on musical theatre, that my body would have to give up first before I do! But, I do have some hopes for the future. They’re not plans, more just things that I’d like to do, and I’m going to work hard and take care of myself so that I can do everything I can in order to be able to achieve them!
 
After NIDA, I would like to keep performing and want to make my professional debut. A dream of mine is to be in SIX The Musical, and I’d also really like to play Beth March again someday. A real big dream is that I want to make the musical theatre industry better than before I entered it, and in relation to that, I’d love to do accessibility and disability consulting for places and shows! 
 
Outside of theatre, in the light of recent events, I want to become a better advocate for my community, for chronically ill and disabled people but in particular help raise awareness for those with ME/CFS, a condition I was misdiagnosed with. When I was sick, it was my friends who have ME/CFS who got me through. Even as I got the right diagnoses and treatments and got better, they’ve stuck by me, cheering me on throughout this journey. I questions what to do if get to pursue my dreams while they get sicker, while I watch more people die from this condition because of a lack of awareness, treatment and medical neglect, knowing it could so easily be one of my loved ones next. I want to use whatever platform I have to help, because no-one is listening outside of the people who are affected, and I know I certainly didn’t before I was diagnosed with it myself.
 
Most of all, I want to keep finding happiness, to stay true to my values and continue being kind and care for others even when it’s uncomfortable or upsetting, and keep still in my belief that the world and people are good no matter how bad things might get.

Our Artists of the Month Gallery

Wondering who we’ve highlighted in the past? Scroll through our gallery of artists below!

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