Contact Our Support Team
Looking for information or guidance on where to find support? We’re here to listen.
Living with Multiple System Atrophy (MSA), supporting a loved one or navigating a recent diagnosis can bring many questions.
At National MSA Research, we understand that finding reliable information and knowing where to look for assistance can sometimes feel overwhelming.
Our volunteer team welcomes general enquiries from people living with MSA, their families, carers and members of the wider community.
While we are not a medical or clinical support service, we aim to help people find appropriate information and publicly available resources.
How We May Be Able to Help
Understanding MSA
If you’re looking for general information about Multiple System Atrophy, we can direct you to educational materials and resources available through our website.
Finding Support Services
We can help you locate information about Australian organisations and services that may provide healthcare, disability, aged care, carer or community support.
Eligibility and access to these services are determined by the relevant providers.
Patient & Family Resources
Our Patient & Family Toolkit is being developed to provide practical information and planning resources for individuals and families.
We welcome enquiries about our available public resources.
MSA Awareness & Community
If you’d like to learn more about our awareness activities, community initiatives or ways to connect with National MSA Research, please contact us.
Research Information
We welcome general enquiries about our research mission and publicly announced research initiatives.
Specific clinical trial eligibility, research participation and treatment questions should be directed to the appropriate research institution or healthcare professional.
Send Us an Enquiry
We’d be pleased to hear from you.
You can contact National MSA Research through our website contact form.
Please provide your name, contact email and a brief description of your enquiry.
Our volunteer team will review your message and respond when available.
Send an enquiry using our contact form
As a volunteer-run organisation, response times may vary. We cannot guarantee an immediate response.
Important Medical Information
National MSA Research does not provide individual medical advice, diagnosis, treatment recommendations or clinical referrals.
If your enquiry relates to symptoms, medication, treatment or an urgent medical concern, please contact your GP, neurologist or another appropriately qualified healthcare professional.
For non-emergency health information in Australia, you can contact Healthdirect on 1800 022 222.
In a medical emergency, call Triple Zero (000).
Your Privacy Matters
We respect the privacy of people who contact our organisation.
Please avoid submitting sensitive medical records, detailed health histories, identification documents or other confidential information through our general contact form.
Any personal information collected will be handled in accordance with our Privacy Policy.
Other Enquiries
For donations, fundraising, sponsorship, volunteering, events or general organisational matters, visitors can also use our main Contact page.
Contact Details
National MSA Research
Rare Neurological Disease Research Ltd
ABN: 55 681 229 032
Email: info@nationalmsaresearch.org.au
Website: www.nationalmsaresearch.org.au
Thank you for reaching out to National MSA Research. Through information, awareness and shared understanding, we hope to help people affected by MSA feel more connected and informed.