Behind The Mic

my journey with IBD

For many, getting a diagnosis is a long, frustrating journey—one filled with pain, dismissal, and self-doubt.

I know this struggle firsthand. After years of being told my symptoms were just stress or food intolerances, I nearly lost my life before finally learning the truth. If you’ve ever felt unheard or alone in your battle with IBD, you’re not. Keep reading! There is hope, and there is a way forward.

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For years, I lived in pain. Exhausted, scared, and constantly dismissed by doctors who chalked my symptoms up to stress or food intolerances. It started after the birth of my second daughter in 2016: bloating, bathroom urgency, unbearable pain. I followed every bit of advice, cutting gluten, tracking food, going low-FODMAP, but nothing helped. I dropped below 50kg, looked visibly unwell, and still, no one listened. Deep down, I knew something was seriously wrong, but I began to blame myself.

After multiple ER visits and being sent home with painkillers and vague advice, my world shrank. I avoided travel, wore nappies for school drop-offs, and lived in fear. The lowest point came in 2023 after my third baby, I collapsed from severe bleeding and was rushed to hospital. Again, I was dismissed. Until I nearly died. A sigmoid scope finally revealed severe Ulcerative Colitis. I later learned signs had been missed years earlier.

That experience changed everything. I became an IBD advocate, speaker, and now, author. Determined to make sure no one else feels as lost and alone as I did. The Ultimate IBD Handbook is the guide I needed: full of real stories, practical tools, and support tailored to the Australian system. If you’re navigating IBD or supporting someone who is, there is hope, there is help, and you are not alone.

The IBD community has needed a book like this for so long. It tackles the tough conversations, fights stigma, and encourages people to take charge of their health. It’s informative, yes but also empowering and uplifting.
Tom W.

IBD Advocate

Living with IBD has fuelled my passion for raising awareness and educating others about the disease. I’m available for public speaking engagements and media appearances to share insights, break stigmas, and advocate for those affected.