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
- Press Releases
- Stakeholder Events
- Uncategorized
- Young People with MS
2017 goals: MS registry and national representation
The Bulgarian MS Society announced it has obtained the status of administrator of personal data under national law. This paves the way for the realisation of two long-awaited projects: setting up a registry of patients with multiple sclerosis and achieving the formal status of representative organisation at national level.
Availability issues for approved drugs. Case study: Nabiximols
By Harriet Doig MS Ireland includes the availability and reimbursement of MS drugs among its priorities as a patient organisation….
Providing modern MS rehabilitation
By SPEM The Portuguese MS Society (SPEM) plans to relocate, expand and modernise the only rehabilitation centre in the country…
No crutches, no benefits: The disability assessment battle
By Alina Verbnîi There are many battles facing people living with multiple sclerosis. In the Republic of Moldova, one of…
MS physical activity platform launched online
By Sandra Fernández The patient organisation Multiple Sclerosis Spain (EME) moved its popular Platform for Promotion of Physical Activity…
MS diagnosis testimony: I feared it was cancer
By Labinot Demi My name is Labinot Demi, I live in Kosovo and I was diagnosed with multiple sclerosis in…
