News

03.10.2018

The journey of a medicine to the market

By our Young People’s Network member & guest author: Jacobo Santamarta Barral (AEDEM, Spain) Have you ever wondered about how…

Restriction on second-line treatment lifted in Poland

28.02.2018

By: Yves Brand Restriction on second-line treatment lifted in Poland Good news from Poland where this week the Polish government…

Restriction on second-line treatment lifted in Poland

28.02.2018

By: Yves Brand Restriction on second-line treatment lifted in Poland Good news from Poland where this week the Polish government…

14.12.2017

Croatia: fighting to end roadblocks for MS patients

By: Tanja Malbasa, Project Manager, Association of Multiple Sclerosis Societies of Croatia The Association of Multiple Sclerosis Societies of Croatia recently…

Nordic youth making their dreams alive: A film on resilience and determination

14.12.2017

“My dream is alive” is a short film co-produced by the Nordic countries’ youth representatives in cooperation with Nerd Productions….

Rising with the sun—a personal story on dealing with the impact of heat

18.10.2017

By: Madeleine Cutting (Asociación Española de Esclerosis Múltiple AEDEM) Many European countries experience scorching temperatures in the summer. When temperatures…

11.04.2017

Football and MS: A story from Croatia

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.

Introducing the underwater ‘barracuda’ wheelchair

10.04.2017

By Pavel Zlobin The Russian MS Society explores novel ways of expanding the mobility for people living with multiple sclerosis….

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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