What is the Atlas of MS?
The Atlas of MS is the most comprehensive worldwide study of the epidemiology of MS and the global availability and accessibility of resources for people with MS.
years is the average age of an MS diagnosis.
of people with MS are women.
people are living with MS. This equates to 1 in every 29,000 people.
people under 18 years are diagnosed with MS in the 55 countries that were able to provide pediatric data. Information on pediatric MS is not available for this country.
people are diagnosed with MS across the globe each day - that's one person every 5 minutes. Data on the number of people diagnosed each year are not available for this country.
* number based on 75 reporting countries
of people are initially diagnosed with relapsing-remitting MS. 5% have progressive MS.
neurologists who specialise in MS. This means there is 1 MS neurologist for every 86 people with MS
nurses who specialise in MS. This means there is 1 MS nurse for every 300 people with MS
In the Atlas of MS we categorise on-label DMTs into three classes: moderate efficacy, good efficacy and high efficacy. Countries should aim to have access to a range of DMTs so that people with MS have options to suit their disease course and individual circumstances.
The Atlas of MS is the most comprehensive worldwide study of the epidemiology of MS and the global availability and accessibility of resources for people with MS.
Access the latest Atlas of MS reports, infographics, slides and datasets to support research, advocacy and policy development. Planning an analysis or publication? Contact the Atlas team at [email protected] for guidance on methodology, data interpretation and related work.
The information in the Atlas of MS can be a powerful advocacy tool, shining a spotlight on MS and raising awareness of the lack of adequate resources available to diagnose, inform, treat, rehabilitate and support people with MS worldwide.
The Atlas of MS relies on data supplied by MS organisations from around the world. We are most grateful to the country coordinators and their colleagues for taking the time and effort to gather the information and data.
The Atlas of MS is one of the strongest examples of what the global MS movement can achieve through collaboration. By bringing together evidence from countries around the world, it helps inform policy, strengthen advocacy and guide future investment in research and healthcare. The Atlas also highlights the need for continued investment in surveillance, registries and data systems to strengthen our understanding of the true burden of MS. Better data lead to better decisions and, ultimately, better outcomes for people affected by MS worldwide.
Professor Mario Alberto Battaglia
Chair, MS International Federation (MSIF) and President of the Italian MS Society (Associazione Italiana Sclerosi Multipla [AISM])