Flush The Stigma

“If your body is telling you something’s wrong, then it’s probably right.” – Elli’s story

It has now been 6 months; I am slowly starting to feel healthy and be able to enjoy my hobbies. I thought the pain I felt was "normal," but I now know it was not. If your body is telling you something's wrong, then it's probably right. I have decided to share my story to help others who feel alone within their diagnosis. 

“I hope to help inspire other teens with IBD and encourage them to share their own”- Maythem’s story

Even though the people around me kept telling me I was faking, I knew something deep inside was wrong. I…

“Remember, you are not alone, and you are doing amazing” – Julia’s story

If I had been told two years ago that I would end up with an ostomy bag, I probably would have cried and not wanted it and would have worried about being “different”. Today, it’s something I’m incredibly grateful for, and for my surgeons and gastroenterologist who listened. There are plenty of support networks out there for those who are struggling and knowing who they are can be a huge help, not just for your physical health but for your mental wellbeing too. Remember, you are not alone, and you are doing amazing.

“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.  

“Keep pushing until someone listens.” – Amelie’s story

Crohn’s is part of my life now. It’s not who I am, but it’s shaped me. It’s made me stronger, more aware, and way more vocal about what I deserve especially in a doctor’s office. If you’re struggling and being dismissed, don’t stop speaking up. You know your body. Keep pushing until someone listens. Because your pain is real. And you deserve to be heard.

“I never could have imagined this would be my life again — taking risks, laughing loudly, living fully” – Jeremy’s story

When I was sick, struggling just to get out of bed, I never could have imagined this would be my life again — taking risks, laughing loudly, living fully.

“I can’t stress enough the importance of advocating for oneself” – Charlotte’s story

Fortunately, through relentless self-advocacy and the search for answers about my condition, I finally connected with a gastroenterologist who truly listened to my concerns. She identified 13cm of inflammation in my colon and diagnosed me with active colitis. My gastroenterologist advocated for me and – since beginning my treatment with Infliximab infusions – I am grateful to be in remission.

“Having to learn to live life in a completely different way takes a heavy mental toll” – Emily’s story

It’s been a long journey to get to where I am today, but I’m proud to say I’m back to feeling strong and fit and pushing myself to do things I never thought possible.

“Keeping your emotions and thoughts bottled up can hurt more than the disease itself” – Josh’s story

To anyone battling UC, or any invisible illness, I want you to know: You are not alone.

“So many people will support you through this journey” – Jennifer’s story

Throughout this process I have learnt that people care about you and are there to support you.

“It’s made me stronger than ever” – Teo’s story

Between 2019 and 2021, I was diagnosed with arthritis, a liver disease and HS skin disease. However, I finally entered into remission this year. It's been one wild ride, but I wouldn't change it because it's made me stronger than ever. I love my Crohn's Disease as it's a part of me.

“It’s important to know when you’re not okay, and to seek help during these times.” – Jackie’s story

For me, it’s so important to have people that I can turn to -to know that I’m not alone. I’d advise people to lean on their support network whenever they can. I’d also suggest doing your own research to remain informed, and to advocate for yourself. It’s important to know when you’re not okay, and to seek help during these times.

Crohn’s & Colitis Australia (CCA)
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