Emma Collin is the Chief Executive Officer of Fight Parkinson’s, which she joined in 2013. Through her leadership, the organisation has become a lifeline of support for thousands of people living with Parkinson’s and their families, delivering tailored professional advice and education to more than 12,000 people each year. Its trusted information resources now reach over 180,000 unique visitors annually, extending Fight Parkinson’s impact well beyond Victoria to communities across Australia.
Emma established Australia’s first multidisciplinary health team within a Parkinson’s organisation and has led its growth to ensure that people living with Parkinson’s and their families have free access to best-practice, evidence-based care. Guided by her commitment to person-centred approaches, Emma ensures services are designed around the lived experiences and voices of people with Parkinson’s. Recognising that many people already receiving Parkinson’s support are later re-diagnosed with Progressive Supranuclear Palsy (PSP) or other atypical parkinsonian conditions, Emma ensured that these communities were formally brought into the Parkinson’s community in alignment with Fight Parkinson’s expertise. By doing so, she has guaranteed that people living with PSP, Multiple System Atrophy (MSA), Corticobasal Syndrome (CBS), and other atypical parkinsonism remain supported, included, and connected to services designed around their complex needs. She has further overseen the growth of a strong professional Community of Practice to build health professional capability in Parkinson’s care.
Nationally, Emma is a Director of the National Parkinson’s Alliance (established in 2024) and a founding member of the preceding National Parkinson’s Action Plan Taskforce. In these roles, she has been instrumental in driving both state and national reform, strengthening services, policy, and systemic change for people living with Parkinson’s and parkinsonism. Internationally, Emma served on the World Parkinson’s Congress (WPC) Leadership Forum Executive Committee from 2016 to 2023 and was appointed Co-Chair from 2019 to 2023. In these roles, she helped shape global collaboration and knowledge exchange, including leadership through the WPC Virtual Congress in 2021 and the WPC Barcelona Congress in 2023.
She is widely recognised for her ability to bring together community, clinicians, researchers, and policymakers to ensure that the voices of people living with Parkinson’s and parkinsonism remain at the centre of reform, care, and research agendas.