A powerful new MS Clinical and Imaging Data Resource, established by the International Progressive MS Alliance, has opened applications for access by researchers.
A new national survey shows the NDIS does not properly understand MS, leading to decisions that impact access to essential care and people’s ability to manage the condition and stay independent.
To mark this year’s National Volunteering Week (18 – 24 May), MS Australia is taking a moment to celebrate the commitment of our Lived Experience Expert Panel (LEEP) members and highlighting what volunteering means to them.
Recent announcements have outlined a series of reforms aimed at slowing NDIS growth, including the introduction of new planning and assessment frameworks, and measures that will significantly reshape how supports are funded, delivered and managed.
CEO Rohan Greenland reflects on Andrea Smith, who lives with MS and recently completed the London Marathon, and how her inspiring effort will be front of mind as he takes on the May 50K.
Two recent studies deepen evidence that Epstein‑Barr virus is central to MS, linking infection to higher risk and improved ways to distinguish MS from related conditions.
10 years on from her MS diagnosis, Kirrily shares her approach to managing her MS with insights from her work as a Physiotherapist.
New studies in experimental models provide potential new avenues for treating or preventing nerve damage in MS.
Australian MS clinicians tell researchers what helps them apply clinical practice guidelines for managing care for people with MS, the barriers they face and their ideas for improving guideline use.
