A Mother’s Mission: Glenda’s Story of Love, Loss and Awareness

Driven by the loss of her son Aaron, Glenda has turned profound grief into purposeful advocacy. As an ambassador for the Australian Melanoma Research Foundation, she is dedicated to raising awareness about the dangers of melanoma and the critical importance of early detection. Through sharing Aaron’s story, at schools, workplaces and within the broader community, Glenda is working to challenge melanoma misconceptions, particularly among young people, and encourage simple, life-saving habits. Her mission is clear: to ensure fewer families experience the heartbreak hers has endured, and to create lasting change through education and awareness.

Glenda at her 70th Birthday Party

Please tell us about your son Aaron as a person.
Aaron was a fit, healthy young man who loved his sport—tennis, footy, always active. But more than that, he was deeply caring. He was strong-willed and determined, yet underneath that was a gentle, thoughtful person. He always looked out for others, especially his disabled brother, often choosing to wait for him, while also encouraging him to hurry up! Family was important to him, and that kindness showed in the small, everyday things he did.

When did he first notice something wasn’t right that eventually led to his diagnosis?
It started with what looked like a cracked heel, like he’d been walking around in thongs for too long. It would bleed and just wouldn’t heal. I remember telling him at Christmas, about a year before his diagnosis, that he needed to get it checked. By Mother’s Day the next year, it was still an issue.
There were multiple misdiagnoses along the way. Doctors thought it was plantar warts. 

“One of the biggest misconceptions is that it won’t happen to you, especially among young people.”

Later, during footy season, he couldn’t run as much as usual and came off the field one game. We noticed a lump behind his knee. That too was dismissed as a benign cyst by doctors. Those delays meant the melanoma had time to spread throughout his body before it was correctly diagnosed.

What do you think are the biggest misconceptions people still have about melanoma?
One of the biggest misconceptions is that it won’t happen to you, especially among young people. There’s still this attitude of feeling invincible, of thinking it’s something to worry about later in life. People continue to sunbake and get badly burnt without realising the risk.
 
There’s also a lack of understanding about how aggressive melanoma is. There’s a lot of public awareness around other cancers, like breast cancer, but melanoma doesn’t always get the same level of attention, even though it can spread very quickly.
 
Aaron created a video to warn others while he was seriously ill. What do you think made his message resonate so strongly with people?
His story really resonated with younger people because they could see themselves in him. At that age, you don’t think something like this can happen to you, but it can happen to anyone.
 
Aaron said “Don’t think you’re bulletproof. Don’t be afraid to discuss problems with your mates and see your doctor on a regular basis. Look out for your mates. Be willing to talk about health with friends and workmates. If you notice someone struggling, don’t let up until they see a doctor. Take note of your body.”
 
Aaron believed his message would help people, and that’s why he did it. It was as simple as that. He wanted others to learn from what he was going through. Read Aaron’s story >>
Losing your son Aaron at such a young age is unimaginable. You’ve spoken about how promoting Aaron’s video helped your healing. Can you share what that process has been like for you?
Sharing Aaron’s story didn’t let me avoid the grief, it meant I had to face the reality of it. I’ve lost two children, and each loss has affected me differently. But speaking about Aaron, going out and telling people what happened, meant I didn’t just keep it all inside.
 
It gave me a sense that I was helping others, especially young people and their parents, not go through what we’ve been through. It felt like, between Aaron and I, we could make a difference. In a way, it helped create meaning from something so horrible.

“Aaron believed his message would help people, and that’s why he did it. It was as simple as that. He wanted others to learn from what he was going through.”

Glenda speaking at the 2015 Melanoma March in Adelaide.
Why do you choose to support the Australian Melanoma Research Foundation and be an ambassador for prevention and early detection of melanoma?
Before he passed, Aaron asked me to keep sharing his video, and I wanted to honour that. I was introduced to the Australian Melanoma Research Foundation through Rachel Sporn, and it grew naturally from there.
 
I started small, doing awareness sessions at my workplace, then at my husband’s workplace, and it kept building. Then I helped instigate the Melanoma March in Adelaide. Over time, people would come up to me and say that hearing Aaron’s story had prompted them to get checked, and in some cases, it saved their lives. That’s what makes it all worthwhile.
 
What are your hopes for the future of melanoma awareness and prevention?
I hope we can change the mindset, especially for younger people. If awareness continues to grow, it can lead to prevention and fewer families having to go through this.
 
Ideally, it becomes something that’s just part of everyday life: putting on sunscreen, being aware of your skin, getting things checked early. Each generation passing that knowledge on to the next.
 
It only takes a couple of seconds to protect yourself with sunscreen. Just do it!

“Aaron believed his message would help people, and that’s why he did it. It was as simple as that. He wanted others to learn from what he was going through.”

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