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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…
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…
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….
