Last week EFNA attended the 4th European Academy of Neurology (EAN) Congress in Lisbon, along with more than 6700 neurologists! Once again, EFNA took this opportunity to bring together our members for our annual General Assembly.
On Day 1 we… Continue Reading
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EFNAOther News
News from EFNA: EAMDA – European Alliance of Muscular Disorders Associations
March 1, 2018EAMDA is the European Alliance of Neuromuscular Disorders Associations and works to support and improve the quality of everyday life of people with neuromuscular disorders (NMDs). -
A “National Action Plan 2025” was launched recently by the Danish government, with broad support from most political parties, and a funding of € 63 mill. for 2017-2019.
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Members of the European Parliament – MEP Interest Group “Brain, Mind and Pain” How the EU can #MakeWorkWork for young people with neurological disorders
Ensuring good work for young people affected by neurological disorders and chronic pain conditions… Continue Reading -
The International Brain Tumour Alliance (IBTA) is a global network founded in 2005 as a worldwide community for brain tumour patient organisations, medical professionals and others in the field of neuro oncology. We bring together international experience and expertise with the aim of enhancing the well-being and quality of life of brain tumour patients and their families and promoting the need for more brain tumour research.
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EFNAOther News
News from EFNA: Meeting of the MEP Interest Group on Brain, Mind and Pain
November 7, 2017November 22, 2017 – European Parliament, Brussels Access to quality healthcare is a basic citizen’s right – yet it is still not a reality for all of us. Large health inequalities persist in the EU and many patients do not… Continue Reading -
EFNAOther News
News from EFNA – European Alliance for Restless Legs Syndrome (EARLS)
October 2, 2017EARLS is a non–profit independent alliance of national Restless Legs Syndrome (RLS - also known as Willis Ekbom Disease) European patient organizations. Launched in November 2009, EARLS had six founding members: Belgium, Finland, Spain, Sweden, The Netherlands and the United Kingdom. France, Norway and Austria have now also joined. -
The European Headache Alliance is a non-profit, patient umbrella group which was launched in 2006. Since then, the Alliance has grown to represent 25 migraine, cluster and other headache disorder patient groups from across the continent. EHA was created to speak on behalf of and to advocate for the rights and needs of the 80 million people in Europe living with a headache disorder.
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2016 was a busy year for the European Federation of Neurological Associations [EFNA], with the launch of some of the organisation's biggest-ever independent projects.
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Over the past number of months, member organisations of the European Federation of Neurological Associations [EFNA] have been profiled in EANpages. Flick back through previous editions to meet those groups advocating at the European level in the fields of Dystonia,… Continue Reading
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Pain Alliance Europe (PAE) was established in November 2011 by a handful of enthusiastic patients organizations from across Europe that wanted to have pain recognised as a disease in its own right.
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Patient Organisation Profile
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EFNAOther News
EFNA Interview with the winner of the Advocacy Award 2016 – Mr. Alistair Newton
April 1, 2017Ann Little (AL): Alistair, congratulations on winning an EFNA Neurology Advocacy Award in the Patient Advocate category. Can you tell us when, how and why you became involved in patient advocacy? Alistair Newton (AN): Thank you. It is an honour to have been chosen for this award, especially as I was part of the 'core' team of the EFNA Board during its formation and through its first decade. In turn, I congratulate the current EFNA leadership on its successes and excellent development since then. -
EFNAOther News
News from EFNA – About DYSTONIA EUROPE – Connecting People for Dystonia
April 1, 2017Founded/Established in and Short synopsis of aims and objectives -
Founded/Established in and Short synopsis of aims and objectives The EPDA is the only European Parkinson’s disease umbrella association. Founded in 1992, we represent national Parkinson’s associations in nearly 30 countries across Europe and advocate for the rights and needs of more than 1.2 million people with Parkinson’s and their families.