Medication
“My friends keep reminding me that I should be proud of myself and lately, I really have been feeling that way.” – Emmie’s story
A few months into traveling, I had another checkup. The results: deep remission. All the hard work, taking multiple daily meds and supplements and working on my diet was all worth it! I cried happy tears in recovery, it had been such a long road back to feeling like myself.
“I still live a good life working and doing things I love doing” – Ronald’s story
At 58 years old I still have trouble with restrictions but with determination I still live a good life working and doing things I love doing.
“I’m reminded that my life isn’t completely ‘normal’ – but that’s okay – it’s my normal.” – Christian’s story
Since starting infliximab I’ve also packed up my life and moved to London for six months. I’ve taken part in a placement program in rural India. I’ve travelled to Bali, Singapore, the UK, Hungary, Greece, Belgium, Netherlands, Spain… I’ve attended the AusGP. I’ve graduated from a Bachelor of Pharmacy. I’ve worked full-time. I’ve studied for and sat multiple exams. I’ve learnt how to cook (or at least am trying to). I’ve made new friends and reconnected with old. I’ve been to concerts and festivals and beaches and parties galore.
“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.
“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.
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!