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EFNA-At-EAN-Congress-2023-Main-Web-1

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 Strategy Revision Position Statement-Post Static

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 Main Image by Mary Doyle

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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Green Illustrated Website Header World MS Day 2023

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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Leda Bresnov - NMOSD - Rare Neurological Disease

NMOSD – A Rare Autoimmune Disease Personal Story – Leda Bresnov

Patient Perspective on Brain Health Series NMOSD – A Rare Autoimmune Disease Personal Story   In 2018 without warning, apart from numbness in my fingers […]

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