• MS Data Alliance in 2019

    One of the main objectives of the ‘Multiple Sclerosis Data Alliance’ (MSDA) is the implementation of a minimal data set and quality standards, approved by the European Medicine Agency (EMA), in as many MS data registries and cohorts as... read more

  • Paediatric MS Workshop in Brussels

    On 27 September 2019 we gathered key stakeholders - informal Caregivers, Nurses, Neurologists, MS societies, children and young people living with MS, as well as industry partners – into a workshop to strategise the development of a Consensus... read more

  • YPN Series: Daniel’s story from Scotland

    By EMSP Young People’s Network member & guest author: Daniel Lafferty Daniel’s life changed forever when he got diagnosed with multiple sclerosis (MS) at age 15, but he learned how to build the momentum of change himself. Another aspiring... read more

  • EMSP at ECTRIMS 2019: 11-13 September, Stockholm, Sweden

    ECTRIMS brings newest MS research to Stockholm The 35th ECTRIMS (European Committee for Treatment and Research in Multiple Sclerosis) Congress is just around the corner. From 11 to 13 September 2019, ECTRIMS, the world's largest annual... read more

  • Research and innovation: 13 things people with MS expect from N2B-patch

    In 2017, an innovative project called... read more

  • 10 things you need to know about the EU Elections if you voted for health

    At the European Elections in 2019 (24-26 May) you might have opted for politicians or political parties who are active on health issues, who will be able to fight in the European Parliament for more health in Europe and help us move forward our... read more

  • Highlights of the #EMSP2019: A young MSer’s Perspective

    By our Young People’s Network member & guest author: Amandeep Donna Nahal (UK MS Society) The Wait is Over May 9th, 2019 and I arrived in beautiful Vilnius, Lithuania for EMSP’s Annual Conference 2019.  This year’s theme was Digital... read more

  • YPN Series: Helen’s story from Hampshire, UK

    By EMSP YPN member & guest author: Helen Chandler (Hampshire, UK MS Society) Last month EMSP’s Young People’s Representative, Patrik Puljić shared with us how he’s been doing as a member of our Executive Committee for the last nine... read more

  • YPN Series: Patrik’s story from Croatia

    By EMSP Executive Committee member & guest author: Patrik Puljić (Croatian MS Society) Patrik Puljić from Croatia was elected as the young people’s representative to the EMSP Executive Committee during the Annual General Meeting in 2018... read more

  • Innovative Drug Delivery Treatment for Multiple Sclerosis

    The N2B-Patch is a project funded by the European Union, which brings together universities, research institutes, SMEs, industry and patients organisations to explore the possibility to have treatments (in MS) that bypass the Blood Brain Barrier... read more

  • Accessibility & perfect summer break? No longer fantasy

    Are you longing for an accessible holiday this summer? Now we have good news for you!... read more

  • World MS Day 2019

    “MS is the same for everyone”. This and other myths about MS are busted as part of the World MS Day 2019 campaign. On the 30th May, #MyInvisibleMS campaign is raising awareness of the invisible symptoms of MS and the unseen impact they have on... read more

  • EU Elections EMSP Campaign

    Less than three weeks until the EU Elections: Vote for health!

    "Democracy is not just the right to vote, it is the right to live with dignity" Use your vote in the upcoming local & EU Elections! There is power in the MS community. Everyday MS allies support one another, work to improve the lives of people... read more

  • MS Nurse Pro Launch event in France

    Continuous training for specialised multiple sclerosis nurses available now for French caretakers We announce with great joy that on April 16th 2019, the MS Nurse PROfessional accredited e-learning training curriculum was officially launched in... read more

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