Youth
My Decade with Crohn’s – Malachy’s Story
Ten years later, I’m 20 now and know how to explain and openly talk about my Crohn's so my mind and stomach can feel at peace.
Navigating My Life with Crohn’s Disease – Devin’s Story
To anyone living with IBD, remember you’re not alone. With support, self-care, and hope, anything is possible!
How a Young Girl with Crohn’s Became a Nurse – Dana’s Story
Helping others with similar stories and health conditions makes me feel like I can make a difference in this world even if it’s just one person.
Finding Clarity After Uncertainty – Hannah’s Story
Being repeatedly dismissed made me feel invisible, like I was fighting something serious on my own.
“I want to be part of the movement that breaks the stigma and makes sure no one feels alone and confused the way I once did.” – Amani’s story
IBD has reshaped me in ways I never expected. It has pushed me to be more ambitious, more resilient, and to pursue studies in nutrition and dietetics so I can one day make a meaningful impact for others living with IBD.
“Through all of it we have no choice but to go on with our days” – Svetlana’s story
For the last 9 and a bit years, I’ve only been in remission from my disease for one of those years. I’ve missed out on so many opportunities and general enjoyment because of this disease taking over my life.
Our Journey with Ella and Charlotte
Both of our daughters, Ella (13) and Charlotte (9), have been diagnosed with Crohn’s disease. It’s been a journey of heartbreak, strength, resilience, and learning—for all of us.
“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
“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.
“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.
“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.
“The unseen battle” – Jazmin’s poem
A war within, Raging Silently, In the depths of my being, Crohn's, an unwelcome guest, Tearing through my insides