for-associations

For Patient Associations.

A series of online webinars made throughout Europe to inform about COVID19 and migraine.

Join The Migraine Movement!

The only worldwide movement that works to improve patients migraine life.

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For Patient
Associations.

A series of online webinars made throughout Europe to inform about COVID19 and migraine.

Join The Migraine Movement!

The only worldwide movement that works to improve patients migraine life.

Previous slide
Next slide
WHAT CAN EMHA DO FOR PATIENT ASSOCIATIONS.

Being a member of EMHA

EMHA works together with its members to give voice to all migraine and other headache patients. We give our members tools and resources for them to become stronger patient’s associations, increasing their visibility and building a community capable of helping their local patients.

By conducting studies, research and strong communication actions we aim at mobilizing the community, to strengthen our work with policy makers and spread reliable information which will help EMHA’s members make an impact in their communities.

TALKS ABOUT MIGRAINE AND CH

Being informed is the first step to be more protected.
#TogetherTalks

2021
Together Talks on Migraine and Access to treatment feat Migraine Association of Ireland

2021
Together Talks on Migraine and Access to treatment feat The Headache Foundation and Migraine League.

2020
Together Talks: On Migraine and COVID-19. feat. MIGRA Portugal

2020
Together Talks: On Migraine and COVID-19. feat. The Migraine Trust

2020
Together Talks: On Migraine and COVID-19. feat. Migréna-help

2020
Together Talks: On Migraine and COVID-19. feat. AEMICE

The Migraine Movement

TOOLKIT

All the necessary assets for spreading The Migraine Movement and building a strong patient’s community. 

movement-logo
EMHA PROJECTS

Raising awareness to change the future under #TheMigraineMovement

Stigma survey 2023

Migraine & Stigma Survey 2023 In 2023, the EMHA conducted a comprehensive pan-European digital survey answered by 4.210 people across 17 countries. In order to examinate the origins of stigma surrounding migraine, its impact on patients, and their need for better understanding and support. The survey covers various topics such as patients’ ease in sharing

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Access to care survey 2021

The EMHA worked along KPMG on a market research to understand the patient journey and burden of disease for migraine in 12 countries. The Access to care survey 2021 has shown insightful results on the patients’ access to treatment and care in each of their country. Summary of the “Access To Care III” survey results

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Women at work

In 2018 EMHA organised a survey among migraine patients working in 7 EU countries (Ireland, Italy, France, Germany, Portugal, Spain and United Kingdom.
The survey shed light on how women have to juggle between migraine attacks and work.

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The Migraine Assistant

After launching The Migraine Movement Manifesto, from EMHA, we set the goal to inform the largest amount of European migraine sufferers about the existence of that movement, born with the aim of giving them visibility, answers and support.

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Explaining Migraine

We realized that the words we normally use to describe our relationship with migraine simply fall short to convey the true feeling behind. Words like “pain” or “horror”, commonly used to describe a migraine, ended up being generic adjectives that linked our disease to a simple headache.

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The Missing Lesson

The lack of medical training is the main barrier for an accurate diagnosis when a possible migraine patient first visits a doctor. In the world, only 4 hours of migraine are studied in medical training.

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ANNUAL REPORT

EMHA Activities Report 2022

EMHA’s agenda of 2022 was filled with trips, meetings and events that put migraine on the agenda of European’s and worldwide organizations and policy makers.

Finance Report 2022

EMHA’s finance report of annual incomes and expenses.

OUR MEMBERS

33 Patients associations
from 24 European countries.

EMHA is compound by more than 33 European migraine and other headache patient associations. Together, we help our members reach new patients and build stronger communities.

We work along our members spreading knowledge on migraine, fighting the stigma society has on it and offering useful tools for all European headache patients to achieve a better quality of life. 

Join our community of migraine and other headaches patients associations.

AGENDA

Don’t miss our upcoming events.

21 June

ShadesForMigraine

29nd June - 2nd July

European Academy of Neurology Congress – Helsinki

1 July

Stigma Scientific Committee Meeting – Helsinki

5 - 8 September

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