The Atlas of MS is inspiring countries to tackle MS-data gaps. Find out how MS organisations are harnessing the power of data to advocate for change.
Studies provide insight into the links between MS prevalence, severity, latitude and healthcare spending
Register now for the ‘Atlas of MS – The Power of Data’ webinar to find out how two MS organisations who lacked data, tackled this issue and the lessons they learnt along the way.
22 July – join the conversation this World Brain Day
The clinical management part of the Atlas of MS is now available
Driving global change - progress made by the global MSIF movement
The 3rd edition of the Atlas has been released
Research suggests a rise in the number of people estimated to be living with MS in the UK.
People with MS, caregivers and MS organisations from across the world come together
MSIF’s Atlas of MS with new data on the number of people living with MS across the world, and the challenges they face.