Your Account
Sort
Categories
- #EMSPVirtual2021
- Associate members
- Document
- EMSP Events
- EMSP Events|EMSP News
- EMSP News
- EMSP News|From Europe
- EMSP News|From Europe|Stakeholder Events
- EMSP News|MS Research
- EMSP News|Press Releases
- EMSP News|Young People with MS
- From Europe
- From Europe|Member News
- From Europe|Stakeholder Events
- From Europe|Young People with MS
- Full members
- Full members|Member News
- Member News
- Member News|Young People with MS
- MS Research
- News – EMSP
- News2
- Press Releases
- Project Updates
- Stakeholder Events
- Uncategorized
- Young People with MS
Portugal is dancing to support people with MS
National MS Society of Portugal (SPEM) launched an initiative to value the capabilities of people with disabilities, fight prejudice and highlight the importance of social integration. This advocacy campaign calls public attention to Multiple Sclerosis and the cause of people with MS.
Restriction on second-line treatment lifted in Poland
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
By: Yves Brand Restriction on second-line treatment lifted in Poland Good news from Poland where this week the Polish government…
Nordic youth making their dreams alive: A film on resilience and determination
“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
By: Madeleine Cutting (Asociación Española de Esclerosis Múltiple AEDEM) Many European countries experience scorching temperatures in the summer. When temperatures…
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.
My MS, My Needs: 1 in 3 people without care and support
By Georgina Carr The UK MS Society’s My MS, My Needs 2 survey of over 9,000 people with MS in England shows…
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.
