Access to rehabilitation or other therapies for symptom management Rehabilitation or therapy available in country of interest? World Bank category Upper middle income WHO region Americas Global results
% of countries reporting people can access rehabilitation or other therapies for each symptom
Fatigue Yes 54% 59% 59%
Heat sensitivity No 21% 41% 25%
Difficulty walking Yes 96% 100% 93%
Stiffness and spasms Yes 93% 94% 91%
Bladder problems Yes 68% 82% 73%
Memory and other cognitive problems Yes 57% 88% 57%
Pain and other unpleasant sensations Yes 68% 88% 77%
Emotional and mood problems Yes 68% 94% 69%
Vision problems No 36% 65% 52%
Dizziness or vertigo Yes 57% 88% 63%
Bowel problems No 57% 88% 56%
Tremors No 50% 71% 55%
Sexual problems Yes 43% 76% 51%
Difficulty moving arms/hands No 79% 88% 80%
Swallowing problems Yes 68% 88% 71%
Speech problems Yes 75% 94% 74%
Seizures Yes 57% 88% 60%
Not sure No 4% 0% 4%

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.

Explore the latest MS data

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.

Powerful tool for change

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.

With thanks to…

Worldwide collaboration

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.

See contributor list

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])