Shane Wormald’s Silicosis Story | Silicosis Support Australia

“You can’t see it, but it’s there”: Shane Wormald’s story of silicosis and survival

A voice from underground, and a warning for others

Shane Wormald, tunnelling veteran and silicosis advocate, sharing his story.

For over 30 years, Shane Wormald worked in Australia’s tunnelling and mining industries. The hours were long, the conditions tough, but the rewards were worth it—or so he thought at the time.

Shane was proud of his work, and proud of the infrastructure he helped build. But what he didn’t know then was that every day, while cutting through rock and dust, he was breathing in something far more dangerous than it looked.

In a new episode of Dust Disease Diaries, Shane shares his story—his work, his diagnosis, and the difficult road that followed. His voice is calm, but his message is urgent.

A hidden exposure, years in the making

In the early 90s, Shane entered tunnelling to provide for his young family. There was little awareness back then about the dangers of fine silica dust. Even with masks and ventilation in place, the particles that caused the most harm were invisible. Workers were never told just how serious the risk could be.

For Shane, the symptoms didn’t show up straight away. But when they did—shortness of breath, chest tightness, fatigue—he was misdiagnosed with sarcoidosis, a relatively benign lung condition. By the time his true diagnosis came, the damage was already done.

The diagnosis that changed everything

In 2016, Shane was officially diagnosed with silicosis, as well as chronic obstructive pulmonary disease and rheumatoid arthritis. The diseases were the result of years of unprotected silica dust exposure.

This diagnosis had a profound impact. Not only did it affect his physical health, but it also challenged his sense of self and his role in the industry. There were surgeries, long periods away from work, and moments where Shane admits he felt overwhelmed and uncertain about the future.

From silence to advocacy

Although initially reluctant to speak up, Shane realised his story could help others—especially younger workers who might not fully understand the risks they face. In 2021, he shared his experience publicly for the first time, and the response was powerful.

He received messages of support from workers and industry leaders alike. Today, Shane works in a leadership role, helping to manage risk on job sites and promote safer practices. He believes that real change comes from awareness, accountability, and better equipment and education.

A personal message to workers and families

In the podcast, Shane speaks directly to those recently diagnosed with silicosis or still working in dusty environments. His advice is clear. Use protection. Ask questions. Don’t wait until it’s too late.

He also shares an emotional message for those struggling after a diagnosis. He acknowledges the mental health challenges, the strain on relationships, and the uncertainty that comes with chronic illness. But he also offers hope, drawn from his own experience of rebuilding his life and mindset.

Listen to the full podcast

Shane’s story is honest, emotional and deeply important for anyone involved in mining, tunnelling, construction or manufacturing. He speaks from experience and from the heart.

Listen to the full episode of Dust Disease Diaries:
Listen to Full Podcast

If you’ve been affected, you’re not alone

If you’ve been diagnosed with silicosis or are supporting someone who has, you don’t need to face it alone. This Silicosis Support Hub provides practical tools, up-to-date medical and legal information, and lived experiences from others who understand what you’re going through.

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