Our MS resources:

Explore MS21's communication tools
and publications below

Conference posters

Bharadia T et al. (2019) Systematic mapping of the global educational offerings for multiple sclerosis patients on the topic of disease progression. Presented at ECTRIMS, Stockholm, Sweden
Vermersch P et al. (2019) A sub-analysis of global mapping data on the availability ofonline educational resources for multiple sclerosis patients. Presented at EAN, Oslo, Norway
​Schippling S et al. (2O18) Comparing patient and healthcare professional perceptions on multiple sclerosis management and care – a sub-analysis of disease progression perceptions. Presented at ECTRIMS, Berlin, Germany
​Schippling S et al. (2O18) MS in the 21st Century mapping study identifying the global educational offerings for multiple sclerosis patients. Presented at ECTRIMS, Berlin, Germany
Oreja-Guevara C et al. (2O18) Patient involvement in treatment decision-making: a sub-analysis of the ‘MS in the 21st Century international unmet needs survey’ comparing patient and healthcare professional perspectives. Presented at EAN, Lisbon, Portugal
​Morrow SA et al. (2O18) A mapping study comparing educational resources for multiple sclerosis patients across the USA, Latin America, Middle East and Asia-Pacific regions [Poster ISO2] Presented at CMSC, Nashville, USA
Rieckmann P et al. (2O17) A mapping study to compare the educational offerings for patients in the fields of multiple sclerosis and HIV in Europe and Canada. Presented at ECTRIMS-ACTRIMS, Paris, France
Rieckmann P et al. (2O17) Comparing patient and healthcare professional perceptions on multiple sclerosis management and care – where do their priorities differ? Results from a qualitative survey. Presented at ECTRIMS-ACTRIMS, Paris, France
Rieckmann P et al. (2O17) MS in the 21st Century Mapping Study to Quantify the Educational Offerings for Patients from Multiple Stakeholders in the Field of Multiple Sclerosis in Europe and Canada [Poster ISO5] Presented at CMSC, New Orleans, USA

Get involved

MS in the 21st Century is proud to base all of its work on original data and insights collected from real people in the worldwide MS community.

If you are a person with MS, a healthcare professional involved in MS care, or a caregiver or family member, please take one of our surveys to help shape future MS in the 21st Century programs.

Get involved

MS in the 21st Century is proud to base all of its work on original data and insights collected from real people in the worldwide MS community.

If you are a person with MS, a healthcare professional involved in MS care, or a caregiver or family member, please take one of our surveys to help shape future MS in the 21st Century programs.