THE HEADACHE AND MIGRAINE COMMUNITY SURVEY
Help us understand the experiences
and unmet needs of people living with headache and migraine.
ACCESS TO CARE SURVEY: GET IMPATIENT FOR MIGRAINE CAMPAIGN
#GetImpatientForMigraine
Access to Care Survey results and campaign.
THE COUNTER
Make your migraine count.
Join the first migraineurs counter and give migraine visibility.
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 appropiate diagnosis and treatment.
READ MORE
For Patients Associations
Working together to give voice to migraine and other headache patients.
READ MORE
For Industry
Improving the quality of life of patients by promoting understanding and visibility of their disease.
READ MORE
For Policy Makers
Making migraine a European health, social and research priority.
READ MORE
For Medical Comunity
Studying, researching and treating migraine and other headaches.
READ MORE
For Media
Raising awareness and spreading reliable knowledge on migraine.
READ MORENEWS
Read our latest news
selected for you.
AGENDA
Don’t miss our upcoming events.
Join 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.
