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
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 rehabilitation, a family programme
By Pavel Zlobin This is a report about the construction and activity of an MS rehabilitation centre. It is also…
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…
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….
2017 goals: MS registry and national representation
By Daniela Shikova The Bulgarian MS Society announced it has obtained the status of administrator of personal data under national…
