National MSA Research
At National MSA Research, we are dedicated to raising awareness, supporting those impacted by Multiple System Atrophy (MSA), and funding vital research into this rare and progressive neurological disease.
As a volunteer-run charity, we work to educate the community, advocate for better understanding of MSA, and provide support through events, outreach, and awareness initiatives across Australia. Through fundraising and community partnerships, we help contribute to research efforts aimed at improving diagnosis, treatment options, and ultimately finding a cure for MSA.
Our mission is to bring hope, connection, and awareness to individuals and families affected by MSA while helping drive meaningful progress in research and support services.


Australian Based. Internationally Connected
At National MSA Research, we are proud to support and strengthen global efforts to improve understanding, awareness, and research into Multiple System Atrophy (MSA). Through our connection with the Global MSA Consortium, we are part of a broader international network of researchers, clinicians, advocates, and organisations working collaboratively to advance progress in MSA research and patient support.
This collaboration helps ensure that Australian voices, patients, and families are represented within the global MSA community, while also allowing us to stay connected with the latest international developments in research, education, and advocacy. By sharing knowledge, supporting awareness initiatives, and fostering collaboration across borders, we aim to contribute to worldwide efforts focused on earlier diagnosis, improved treatments, better care pathways, and ultimately a cure for MSA.
Our involvement with the Global MSA Consortium reflects our commitment to ensuring that no individual or family affected by MSA feels isolated, and that together, through international cooperation and community support, meaningful progress can continue to be made.




