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John and Julie

John and Julie have supported each other and assisted friends diagnosed with Parkinson’s since John was diagnosed 15 years ago.

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They have also raised significant funds for Fight Parkinson’s through the Tulip Ball, been involved in medical trials as well as running a business, travelling, playing competitive sport, being grandparents and sharing lots of laughs.

“You don’t know what life is going to throw at you, so make sure you have fun every day.”

Latest news and resources

Research call-out: The eye as a window into Parkinson’s

Many people with Parkinson’s or RBD experience changes in vision. Early findings suggest that subtle

Advance Care Planning Week 2026: Plan now, peace of mind later

During Advance Care Planning Week (16 – 22 March), Fight Parkinson’s is encouraging everyone in

Multiple System Atrophy (MSA) Awareness Month

What is MSA? Multiple System Atrophy (MSA) is a rare and progressive neurological condition that

Please note: Fight Parkinson’s uses the phrase Parkinson’s rather than Parkinson’s Disease to reflect the community’s preference. Parkinson’s Disease is used only when necessary such as in medical, research or government contents, or in direct quotes.