Support
“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.”
“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
“Ulcerative colitis didn’t just change her life it changed all of ours.”
Ulcerative colitis didn’t just change her life it changed all of ours. We became closer. We became more tired, more emotional, more aware of the fragility of everything. There were arguments. Tears. Long nights of silence. But there was also love so much love. We celebrated the little victories: a full week without pain, a good doctor’s report, a laugh in the hospital room. Those moments meant more than any birthday party ever could. We learned how to fight together. How to lean on each other. How to keep hope alive, even when it was flickering.
Bag, baby and bravery – Kate’s story
Recovery was difficult, especially while navigating new motherhood at the same time. But one year on, I’m healthy, active, and grateful to be here. I used to see stoma surgery as the worst-case scenario—but it truly isn’t. I wish I’d known back then just how much life was still possible after surgery.
“Hold on to hope if you can” – Chloe’s story
While my Crohn's is not fully settled, I am happier than ever. I have almost finished my degree in Journalism, I am working in a job that I love and am surrounded by amazing friends and support. I have been able to travel overseas with complications and plan to go on three more trips this year!
“I am not giving up hope”- Kasey’s story
I am not giving up hope and want to share my story with others who may have similar symptoms and feeling completely lost. Please seek specialist help from a gastroenterologist who is specially trained to help people with IBD. Reach out to others in IBD groups because having someone to talk to that can relate to you is invaluable for your mental health. You are not alone, it’s just sad many do not share their story.