Got Guts
“I have learnt so much about myself” – Bridie’s story
My experience with Ulcerative Colitis (UC) began long before I had a name for it
“You deserve a medical team that listens and investigates” – Elle’s story
While life is not completely the same as it was before diagnosis, it’s a new normal I can count on. I’m stronger, supported, and finally in control.
“Together we can break the silence surrounding IBD” – Natasha’s story.
This is something I feel so truly passionate about, due to the personal impact this disease has had on my life since age 11. I felt I needed to spread awareness in my own way
“Crohn’s might be a part of my life, but it doesn’t get to define it.” – Tahlia’s story
Crohn’s might be a part of my life, but it doesn’t get to define it. I am still me – just a little stronger, a little tougher, and a lot more determined than before.
” You are more resilient than you know” – Amelia’s story
Today, I’m in remission. I still face challenges, but I’ve learned to listen to my body, advocate for myself, and celebrate every small victory.
“Because Crohn’s is a permanent part of our lives and we’re not going anywhere” – Taylor’s story
I have been able to get back into my passions of live music and creating art - something my body wouldn't let me do for a long time. I have recently started looking into IBD support, and it's sad the lack of support for us.
“I still face challenges and anxiety around my disease, but I don’t let it take over my life” – Ellah’s story
It was super difficult trying to navigate life being diagnosed at only 17 years old. Even though I had so much support from doctors, my family and my friends, it was mentally and physically exhausting. Shedding light on this terrible disease is so important so people can realise how much of a struggle having IBD really is. At the same time, you can’t let it control your life.
“Despite everything I’ve kept pushing” – Jaiah’s story
Crohn’s is invisible. From the outside, I look fine. But this disease is exhausting, painful, and relentless. And worst of all, many people think we’re “faking it.”
“You can push and challenge yourself to achieve everything that you want to” – Tara’s story
The hardest time for me was when my medications stopped working in 2021. I was in pain from the moment I woke up, which was both physically and emotionally crippling, as I am normally so active and positive. I wanted to keep up the strong mindset and continue to move my body, but I felt so weak at the time. With the success of Stelara, I now know how much of a privilege it is to feel well and to be able to move my body without limitation. It is for this reason that I have decided to set myself a goal to run 10km in the Nike Melbourne Marathon, where I will be fundraising for Crohn's and Colitis Australia.
“I’m able to make the most of my life with the people I love” – Jas’ story
Sharing my story is important to me because this disease can be very isolating. Whether you've just been diagnosed or you've had it for years. It's encouraging to hear other people's stories and know that you are not alone on this journey.
“I was made to think it was all in my head for so long” – Simone’s story
My mental health and physical health have suffered for years now. I will soon start my journey with biologics. I have a giant fear of needles but I’ve never been so excited to hopefully experience remission.
Living Fearless with Tim
I do it for anyone else out there that is battling Crohn's and colitis. I know how hard it is, and also how hard it can be to talk about it and to feel understood