Migraine & Stigma Survey 2023
The EMHA conducted a European survey to learn how stigma surrounding migraine has an impact on every day life.
DO YOU REALLY KNOW YOUR EMPLOYEES?
1 in 7 workers suffer from migraine. Find out how many workers at your company are suffering from it by doing the test.
ACCESS TO CARE SURVEY: GET IMPATIENT FOR MIGRAINE CAMPAIGN
#GetImpatientForMigraine
Access to Care Survey results and campaign.
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European Migraine
and Headache Alliance
ABOUT EMHA
The European Migraine & Headache Alliance is a non-profit association of patients, that works as an umbrella of different patient groups around Europe. The Alliance was launched in 2006 and since then, we represent more than 33 patient groups across the continent.
EMHA is an active member of the European Federation of Neurological Alliances [EFNA], the International Association of Patient Organizations [IAPO], the European Patients Forum [EPF] and also works closely with different organizations such as the European Headache Federation [EHF], European Brain Council [EBC] among others.
EMHA Associations
EMHA is a non-profit umbrella organization with 34 patient associations for Migraine, Cluster Headache, Trigeminal Neuralgia and other headache diseases, across Europe.Â
EMHA Associations
EMHA is a non-profit umbrella organization with 34 patient associations for Migraine, Cluster Headache, Trigeminal Neuralgia and other headache diseases, across Europe.Â
FOR YOU
EMHA is a patient organisation alliance
formed by 33 members.
Find out more on what we can do for you.
For Patients
Improving patients access to appropriate diagnosis and treatment.
READ MOREFor Patients Associations
Working together to give voice to migraine and other headache patients.
READ MOREFor Industry
Improving the quality of life of patients by promoting understanding and visibility of their disease.
READ MOREFor Policy Makers
Making migraine a European health, social and research priority.
READ MOREFor Medical Community
Studying, researching and treating migraine and other headaches.
READ MOREFor Media
Raising awareness and spreading reliable knowledge on migraine.
READ MOREJoin the movement
If you are a patient, you can share your experience with us, your motivation and your desire to change the actual situation. If you are the family member of a migraineur, you also have a great deal of experience to share and an empathy feeling to work on.
If you are a healthcare professional, you can deepen your knowledge of our situation and help us live a better life.
If you are an employer, you can put yourself in our place and help us build a more fair and safe society for millions of workers in Europe and all over the world.
If you are a politician, we expect you to join our cause and cooperate with us to reach goals that otherwise would be unreachable without you.
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