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Larissa's Story
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When my daughter was born, I expected the usual challenges of new motherhood: broken sleep, endless feeding, and the emotional ups and downs everyone warns you about. What I never expected was that six weeks later I would be sitting in a hospital room, holding my tiny baby, hearing the words, “Your baby has cystic fibrosis”.

In that moment, my whole world tilted.

The future I had imagined for her suddenly felt fragile. One day I was learning how to settle a newborn and the next I was learning how to manage a lifelong medical condition. My life filled overnight with medical terminology, tests, medications, enzymes, airway clearance, and more hospital appointments than I could count. Everything felt unfamiliar, intimidating, and impossibly heavy.

Everyone was focused on my daughter, which made sense. But what no one saw was what was happening quietly inside me.

The shock, the fear and the grief that I didn’t know how to name. The sense of losing control over something as precious as my daughter.

Those feelings didn’t fade. They seeped into every part of my early months as a mum. My sleep suffered. My confidence crumbled. I struggled to connect, not just with my baby, but with my husband, with myself, with the world around me.

Some days even breathing felt like a task. Other days I ran on autopilot, doing everything I was ‘supposed’ to do while feeling completely detached. There were moments of anger, too. Why her? Why us? I felt overwhelmed by the responsibility. Terrified of making the wrong choices. Alone in a world that no longer made sense.

This wasn’t just ‘new mum worry’. This was postpartum depression, but I didn’t have the words for it yet. I just knew something inside me didn’t feel okay.

Somewhere in the middle of all that chaos, our community nurse handed me a flyer for Gidget Foundation Australia. I remember staring at it for days before I finally reached out. Asking for help felt scary, but it turned out to be one of the best decisions I’ve ever made.

When I connected with Gidget Foundation Australia, something inside me softened. For the first time, I felt truly seen. Not just as a mother facing a medical diagnosis, but as a person carrying trauma, fear, and overwhelming emotional weight.

With my Gidget Clinician, I had a safe space to speak honestly. To cry, unravel and learn to rebuild.

They gave me tools to help manage my emotions and start piecing myself back together. They helped me understand that what I was feeling wasn’t rare and wasn’t a personal failure. It was valid and it was common. 

My Gidget Clinician helped me realise I didn’t have to be ‘strong’ every minute of the day. What I needed was support, not perfection. Their care didn’t just help me, it made me a better mother for my daughter and a better partner to my husband.

My daughter’s cystic fibrosis diagnosis changed our lives forever, but it also taught me something powerful - asking for help isn’t weakness, it’s courage.

My story isn’t only about a diagnosis. It’s about resilience. It’s about healing. It’s about the importance of compassionate, accessible perinatal mental health care.  And it’s a reminder that no parent should ever walk this path alone.

Larissa's Story

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