Please visit https://t.co/6Cf1jOAbeW to learn more about Peter’s journey with Parkinson’s and donate to help someone else navigate a system that can feel overwhelming. 💙
Did you know…? The NDIS application for people who live with Parkinson’s is over 50 pages long.
“I didn’t know how to navigate the system,” says Peter.
But Fight Parkinson’s was there to lend Peter a hand, and he was guided on how best to explain his Parkinson’s within a complex system.
“I wouldn’t have known how to do that without the Fight Parkinson’s multidisciplinary health team. They guided me through it.”
Our health information service will not be available, however, you can leave a message on 1800 931 031 or email us at [email protected] and our health team will endeavour to respond to your enquiry as early as possible.
In recognition of 🏳️🌈 Pride Month 2026 🏳️🌈 we are pleased to promote the ‘LGBTIQA+ and living with Parkinson’s’ online course, available at no cost, on the Fight Parkinson’s Community Learning Hub.
Whether you’re a member of—or caring for someone who is a member of—the LGBTIQA+ and Parkinson’s communities, or an individual looking to learn more, Pride Month is a great time to educate yourself via the Fight Parkinson’s Community Learning Hub.
Join us for our next Positive Life session on Wednesday 10 June, where we’ll explore ways to manage fatigue and apathy in Parkinson’s.
These symptoms can affect energy, motivation, and day‑to‑day wellbeing, and they are often difficult to navigate on your own.
This session offers clear, practical guidance to help you better understand what’s happening with your mind and body, and find approaches that support you to live well. The session runs from 10:00am to 11:00am online via Teams and is open to anyone who would like to attend.
Please visit https://t.co/T3WkgXBGt2 to learn more about Peter’s journey with Parkinson’s and donate to be the reason someone like Peter receives the support they need when everything feels uncertain. 💙
To wrap up PSP Awareness Month, Fight Parkinson’s is pleased to share a personal story of lived experience from Michelle, and her husband and carer, Mark.
But by leaning into her creative interests to publish helpful resources on PSP for others, embracing normalcy and routine with her husband of 38 years, and accessing the support of an Atypical Parkinson’s peer support group through Fight Parkinson’s,