• MS Sessions 2019 | Bucharest, Romania

    [embed] This year EMSP in collaboration with Shift MS organised the 2nd volume of the MS Sessions! A festival aiming to bring together young MSers from all over Europe. More than 170 newly diagnosed young MSers gathered up in the beautiful... read more

  • Young people’s Network 2.0 Advocacy skills training: Making a change

    From the 27th to the 29th of September,  EMSP organised an advocacy training workshop in Luxembourg, for the Young People’s Network members. The workshop aimed to help young MSers develop the skills and acquire the knowledge to effectively run... read more

  • EMSP Annual Conference 2019

    A ‘to-go-to’ meeting for patients, healthcare professionals, industry, patients’ organisations, policy decision-makers and key opinion leaders in the field of Multiple Sclerosis (MS). This year was a special edition for EMSP, since the... read more

  • What we learned at ECTRIMS 2019 – Part 2

    In October we shared the first part of the most important learnings from ECTRIMS 2019. Having such a wide variety of topics discussed this year, we could not squeeze all the research news into one blog piece. This did not hold us back though.... read more

  • Rethinking MS in Europe

    On 3 December, the International Day of Persons with Disabilities, the European Brain Council (EBC) and the Health Policy Partnership (HPP) launched the RETHINKING MS policy narrative report. This report calls for change in MS care and support... read more

  • MS Nurse PRO launched in Portugal

    On 6 December, the European Multiple Sclerosis Platform and the Portuguese MS Society launched the... read more

  • Scan for change – Belgian MS Ligue joins Payconiq campaign

    What does 2 euro represent for you? A cup of coffee? Your daily newspaper? A quick drink after work? For many of us, 2 euro is just a small amount you might pay as part of your daily ritual. But for some people, 2 euro can make a big difference.... read more

  • MS recipe book developed in Greece

    On 13th November 2019, the Pan-Hellenic Federation of Multiple Sclerosis (POAMSKP) organized a Press Conference for Health Reporters to present the “Nutrition in Multiple Sclerosis - 20 recipes by Dina Nikolaou” recipe book. Appropriate... read more

  • Stop MS Appeal

    Stop MS: MS Society UK launches its biggest fundraising appeal ever   In October the MS Society UK publicly launched its biggest-ever fundraising appeal – the Stop MS Appeal. The Appeal is aiming to raise £100 million over ten years to... read more

  • Insights from the European Health Forum Gastein 2019

    In the beginning of October, EMSP was represented at the European Health Forum Gastein (EHFG), widely known as 'Davos for Public Health', the leading health policy conference in Europe. Since its foundation in 1998, the conference has developed... 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

  • 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

  • What we learnt at ECTRIMS 2019 – Part 1

    This year, 35th edition of the ECTRIMS (European Committee for Treatment and Research in Multiple Sclerosis) Congress was quite hectic and educational for EMSP and its members. Between 11 and  13 September 2019, the... read more

  • 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

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