Tag: data
Get the evidence
Provide information on the number of people with MS and barriers to accessing healthcare to key decision-makers in your country.
MS registries: putting people with MS at the heart of research
MS affects people all over the world. MS registries are one of the many advances in MS research that are bringing us closer as a global MS community and closer to ending MS.
Finding the answers to COVID-19 & MS : Your role in the global effort
Register now: a webinar for people with MS and MS organisations – your questions answered on the COVID-19 & MS global data sharing initiative