Studying, researching and treating migraine
What EMHA can do for the medical community
As an alliance of patient associations, we can learn at the source what the main concerns and pain points of migraine patients are.
Our aim is to work together with the medical community to improve the quality of life of the migraine patient, as well as to advocate for the dissemination of reliable information and promote further research into this disease.
Raising awareness to change the future under #TheMigraineMovement
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
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
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.