Isa Adams
I’ve always believed that even in life’s toughest moments, there’s room for positivity, resilience, and community. When I was diagnosed with Parkinson’s, I knew I had a choice — I could let it define me, or I could respond with action. I chose action.
Living with Parkinson’s means navigating both physical and emotional challenges every day. I understand firsthand how complex the condition can be. But rather than stepping back, I became determined to stay active and to uplift others walking a similar path. That’s what led me to become involved in ParknDance and to champion the idea that movement truly is medicine.
Dance has been transformative for me. Through music, rhythm, and tailored movement, I’ve found not only improved strength and mobility, but also joy, confidence, and connection.
Beyond the dance floor, I’m passionate about supporting Fight Parkinson’s as a community fundraiser. For me, fundraising isn’t just about asking for donations — it’s about inviting people to be part of something meaningful and hopeful.
I also share my story publicly whenever I can. Speaking openly about my experience helps break down stigma, encourages earlier diagnosis, and reminds people that they’re not alone.
I’m proud to stand with Fight Parkinson’s and to contribute in any way I can. My message is simple: keep moving, keep connecting, and never lose sight of joy.
Rod Hadfield
Rod is widely regarded as one of the fathers of hot-rodding in Australia, a title earned through decades of passion, persistence, and belief in the power of community.
Looking back, Rod doesn’t just see cars — he sees people. “It was never just about the vehicles,” he says. “It was about giving people something to be passionate about, something that brought them together.”
In recent years, Rod’s journey has taken a deeply personal turn following his diagnosis of Parkinson’s. Living with Parkinson’s has changed many aspects of daily life, but it hasn’t changed who he is or what he stands for.
For Rod, raising awareness of Parkinson’s is important because he knows how misunderstood the condition can be. He understands firsthand the impact it has on movement, confidence, and independence — but he also knows the emotional toll it takes on families and carers.
Rod’s advocacy comes from the same place as his life’s work: a desire to help others and to leave things better than he found them. “If sharing my story helps even one person feel less alone, or pushes research and support forward, then it’s worth it,” he says.
Rod Hadfield’s legacy is one of passion, resilience, and purpose — proof that even when the road changes, the drive to help others never does.
Marty Rankin
Marty Rankin is a former real estate agent and business owner who built two agencies in Melbourne’s inner west while raising a large, blended family. He is a proud father to Brad (31) and Lily (16), husband to Rachel, step-father to Chloe (32), Olivia (28) and Gabrielle (25), and grandfather to Willow (3) and Hugo (7). Family, connection and showing up for others have always defined his life.
Music is where Marty’s heart lives. As part of a group of professional musicians, he has long believed in the power of music to heal, connect and uplift. In 2022, Marty was diagnosed with Parkinson’s disease — a moment that reshaped his life and sharpened his sense of purpose.
While grateful for access to world-class healthcare, Marty recognised that many Australians living with Parkinson’s in regional and remote communities struggle to access meaningful support. Rather than step back, he chose to act.
In November, his band raised more than $5,000 for Fight Parkinson’s at a fundraising gig in Yarraville, transforming personal challenge into collective action. Since then, Marty and the band have partnered with an exercise physiologist to deliver drumming, singing and dance workshops in communities — activities shown to support brain health and build new neural pathways.
As an ambassador for A Walk in the Park, Marty walks for his family, his community, and every person living with Parkinson’s who deserves hope, dignity and support.
Sean Anderson
I was diagnosed with Parkinson’s disease in March 2017 at the age of 43. Before that, I’d noticed a tremor in my right hand while mountain biking and people commented on a limp I hadn’t realised I had. I assumed it was fatigue or fitness — anything but Parkinson’s. The diagnosis was overwhelming, and the hardest part was the uncertainty of how quickly things might change and how long I’d be able to keep doing the things I love.
I’ve been fortunate that my Parkinson’s is progressing slowly, and I’ve continued working since my diagnosis. Exercise has become essential, with cycling playing a huge role in managing my symptoms. Some days are tougher than others, with stiffness and muscle rigidity making movement challenging, but I’ve learned that medication and regular exercise together make a real difference.
Parkinson’s isn’t only the visible symptoms. There are also fatigue, anxiety, sleep issues and cognitive changes that people don’t always see. Despite this, it’s not a death sentence — with support and adjustments, you can still live a full and meaningful life.
The support of my wife, family, friends and workplace, along with the guidance from Fight Parkinson’s, has been invaluable. I’m proud to be an ambassador for A Walk in the Park to help others feel supported and connected, and to remind people living with Parkinson’s that they are not alone.
John Eren
John Eren was diagnosed with Parkinson’s disease in 2019 — a moment that marked both a profound personal challenge and the beginning of a new chapter. After nearly two decades serving his community as a member of the Victorian Parliament, he made the difficult decision to retire and prioritise his health, while stepping forward as a passionate advocate for people living with Parkinson’s.
His journey began with subtle but persistent symptoms: tingling in his fingertips, reduced arm movement and difficulty buttoning his shirts. When a parliamentary colleague noticed his hand shaking during a presentation, John sought medical advice and received his diagnosis. While unexpected, the diagnosis provided clarity and a renewed sense of purpose. Rather than retreat, he chose to use his voice and experience to support others facing similar uncertainty.
In 2020, John became an ambassador for 27forParkinson’s, sharing his story publicly to break down stigma and foster hope. That same year, his fundraising efforts helped raise $23,000 to support vital research and services. For John, fundraising has never been only about dollars raised — it’s about building awareness, strengthening community and reminding people living with Parkinson’s that they are not alone.
Now an Ambassador for Fight Parkinson’s, John continues to champion research, early diagnosis and stronger support networks for families across Victoria and beyond. Through public speaking, community events and advocacy, he works to amplify the voices of those living with Parkinson’s and encourage others to seek support earlier. His message is simple but powerful: Parkinson’s may change your life, but it does not define it.
