ARCHIVE

ARCHIVE

Jan Bodenbach - Dystonia Patients Perspective

My Dystonia Story – Jan Bodenbach

Patient Perspective on Brain Health Series My Dystonia Story by Jan Bodenbach It was a cold Friday night when my body began to take away everything […]

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EFNA at EAN Congress 2023

EAN Congress 2023 – Event Report

EFNA AT THE EAN Congress 2023 in Budapest 1ST – 4TH July, 2023 EFNA was delighted to be invited to represent the patient’s voice at […]

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joke jaarsma

Forgotten Happiness – Living with Restless Legs Syndrome

Patient Perspective on Brain Health Series Forgotten Happiness – Living with Restless Legs Syndrome I have become used to this, am lying in bed kicking […]

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EU Pharma Revision – Position Paper

Download the EFNA Position Statement On The EU Pharmaceutical Strategy Revision Recently, the European Commission published revision of the EU pharma legislation. A first in two […]

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Gary Boyle – living well with Parkinson’s

Patient Perspective on Brain Health Series Living Well With Parkinson’s Disease I am not entirely sure when it started – that is the thing about […]

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World Multiple Sclerosis Day 2023

We would like to take the opportunity on this World MS Day to help raise awareness for people living with multiple sclerosis (MS) – especially […]

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Orla Galvin EFNA on stage

Event Report: Making Neurology A Public Health Priority

‘Making Neurology A Public Health Priority’ MEETING REPORT & REPLAY Tuesday, May 23rd 2023, 08.00-10.00hrs CET. Despite the knowledge that almost one in three people […]

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BHNC MEP IG May23 Invite V04

Join us in Brussels to make neurology a public health priority

We are delighted to invite you to attend our upcoming event “Building Awareness & Driving Action: Making Neurology A Public Health Priority” in Brussels on […]

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BAW 2023 EFNA Campaign Feat Img

Brain Health Day 2023 – Neurological Patient Issue Awareness Campaign

Brain Awareness Week 2023 EFNA Patient Advocacy Campaign   This year we marked Brain Awareness Week by running a social media campaign to raise awareness […]

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Eva Frostell - Living With Myasthenia Gravis

Living with a rare neurological disease – Myasthenia Gravis – Eva Frostell

Patient Perspective on Brain Health Series My story of living with Myasthenia Gravis (MG), a rare neurological disease The European Union considers a disease as […]

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