PATIENTS ASSOCIATIONS

Managing migraine: A guide for parents by Migraine Ireland

News, PATIENTS, PATIENTS ASSOCIATIONS / By

Managing Migraine : A guide for parents’ is a curation of Nicola Filzmoser experience with having migraine and her learnings from working with world-leading migraine & pain experts.  For several years, Nicola has been working with world-leading migraine experts, patient organizations, and pain charities to advocate for young people and create this course. At Happyr Health, […]

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Give visibility to the affected ones: Interview of Elena Ruiz de la Torre for Migräne magazin

News, PATIENTS, PATIENTS ASSOCIATIONS / By

EMHA at Migräne magazin informs europe-wide about migraine and tries to improve conditions for the sufferers. In this interview Elena de la Torre, Executive Director of EMHA, talks about achievements, actual projects and her personal motivation (to campaign for EMHA). Raising awareness about migraine throughout Europe and improving conditions for sufferers:This is what the European

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New e-learning series on Personalized Healthcare: Women’s Brain Project

MEDICAL COMMUNITY, News, PATIENTS, PATIENTS ASSOCIATIONS / By

As part of EFNA’s Training Initiatives for Neurology Advocates [TINA] programme, a new series of e-learning modules is launched today, on the theme of personalised healthcare. Personalised medicine is a medical model that aims to provide tailor-made prevention and treatment strategies for defined groups of individuals. This usually involves genomics, information technology and patient empowerment. However, at EFNA, we feel

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Essentials by AEMICE: A series of interviews

MEDICAL COMMUNITY, News, PATIENTS, PATIENTS ASSOCIATIONS / By

Within the documentary ‘Essentials: The role of patients’ associations in the health and social system in the COVID era by AEMICE’ we present a series of interviews with the associations. In this interview, AEMICE talks with Elena Ruiz de la Torre on the importance of the patient’s role in the health system. “We have been

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data_on_migraine_days_lost

The math of migraine: news by AbbVie

INDUSTRY, News, PATIENTS, PATIENTS ASSOCIATIONS, POLICY MAKERS / By

The math of migraine: A common denominator.Brett Dabruzzo’s first migraine hit when she was in high school. Pounding headaches and overwhelming nausea weren’t diagnosed as migraine until almost a decade later when Dabruzzo, Pharm.D., director, medical affairs, AbbVie, began working for a pharmaceutical company in its neurology department. A week into her job as a

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Life is meant to be lived, not coped with; just ask those with migraine

INDUSTRY, News, PATIENTS, PATIENTS ASSOCIATIONS, POLICY MAKERS / By

Prioritizing the health and wellbeing of those with migraine is in the best interest of everyone, given the impact the disease has on societies and health care systems as a whole. Imagine going through life coping and not living. A life riddled with anxiety and uncertainty where you feel unable to plan the simplest of

Life is meant to be lived, not coped with; just ask those with migraine Read More »

Portuguese EU Presidency EMHA’s contribution to the EU social summit 2021

News, PATIENTS, PATIENTS ASSOCIATIONS, POLICY MAKERS / By

EU social summit 2021: The Portuguese Presidency of the Council of the European Union is holding a High-Level Conference and an Informal Meeting.  of Leaders at the invitation of the President of the European Council. The Summit will give political impetus to the implementation of the European Pillar of Social Rights and its Action Plan, underlining its

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Women and Migraine: Bringing women out of the shadows

INDUSTRY, News, PATIENTS, PATIENTS ASSOCIATIONS, POLICY MAKERS / By

Brussels, 23 March 2021 Today, EMHA and the European Parliament Migraine Alliance organised a webinar to raise awareness about the hurdles women with migraine have to overcome and call for action. The call for action is embedded in EMHA’s Policy Paper on ‘Women and Migraine: Bringing women out of the shadows’ that was launched at the

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The EP Migraine Alliance, Call to Action: MEPs present their coalition to support EMHA’s advocacy campaign.

Campaign, Events, News, PATIENTS ASSOCIATIONS, POLICY MAKERS / By

On 22 September 2020, the European Migraine & Headache Alliance organised ‘The Missing Lesson’ webinar to raise awareness about migraine at EU level and kick-start its EU policy advocacy campaign to make migraine a European health priority. The webinar focussed on the medical curriculum deficit when it comes to migraine. This leads to under- diagnosis

The EP Migraine Alliance, Call to Action: MEPs present their coalition to support EMHA’s advocacy campaign. Read More »

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