News

15.05.2017

The MS House in the European Parliament

Hosted by MEP Kateřina Konečná, the MS House is a fully immersive experience coming to the European Parliament from 30th…

Event Report: EP debate: Can real world data advance equity of health care?

03.05.2017

People living with multiple sclerosis (MS) in the European Union could receive timelier access to safer and more efficient therapies….

EMSP Newsletter: April 2017

28.04.2017

The fourth EMSP newsletter of the year features updates on our upcoming Spring Conference, includes exciting project and member news,…

27.04.2017

MS Nurse Pro launched in Romania

EMSP’s online training programme dedicated to MS nurses is expanding. MS Nurse Professional was launched in Romania, the 10th country…

EMSP Membership Newsletter: Bringing MS Voices Together

24.04.2017

We are very glad to present the third edition of our Membership Newsletter. With the great support of our members, we aim…

Football and MS: A story from Croatia

11.04.2017

A young and enthusiastic team of multiple sclerosis (MS) advocates living in Zadar, Croatia, have produced a video about one of their own: Patrik, 24 years, diagnosed with MS six years ago.

Patrik is in love with football and after his diagnosis he feared he would not be able to play it anymore. This is a story about some of the key aspects of living with MS.

10.04.2017

Multimedia patient advocacy

The Serbian MS Society (DMSS) is relying increasingly on multimedia initiatives in its outreach to different MS stakeholders, from MS patients to health authorities. Two related activities are the publication of a popular MS magazine and the development of a nationwide video campaign. Article for EMSP’s Membership Newsletter.

Training for MS carers

10.04.2017

By Madeleine Cutting The Spanish MS Society AEDEM organised two training sessions for MS carers – key but often disregarded actors…

My MS, My Needs: 1 in 3 people without care and support

10.04.2017

The UK MS Society’s My MS, My Needs survey of over 9,000 people affected by this condition in England shows that over the past four years demand for social care among persons with MS has increased. Despite this reality, fewer are getting the support they need. Article for EMSP’s Membership Newsletter.

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