Migraine Ireland

Migraine Ireland (Irish: Cumann Mígréine na hÉireann), also known as the Migraine Association of Ireland, is an Irish patient charity and advocacy organisation focused on migraine and other headache disorders. It describes itself as Ireland's only patient charity providing support, education and information for people living with migraine, their families and healthcare professionals. The organisation operates the website migraine.ie and positions itself as an informational and patient advocacy body rather than a medical provider; it explicitly states that it is not a medically regulated entity, does not provide medical advice and does not answer medical queries. Migraine Ireland's mission centres on relieving the burden of migraine through support, self-education, information and resources. It highlights that migraine is a complex neurological condition classified by the World Health Organization as the seventh most disabling disease in the world and the most common neurological condition, affecting roughly 12–15% of people. It notes that migraine is about three times more common in women than in men, is usually inherited, and that attacks can last from 4 to 72 hours, with frequency varying greatly between individuals. The organisation recognises the stigma, misunderstanding, misinformation, health literacy challenges and fragmented, regionally differing healthcare landscape that people with headache disorders may face in Ireland. Its activities include providing accurate informational resources, signposting to services, listening support and occupational advocacy, as well as building public awareness and understanding of migraine and its associated disability. It also aims to be a patient voice in Irish healthcare discussions and supports research into the condition and related medical matters. Migraine Ireland engages with the public through its website, which offers sections for people living with migraine and for healthcare professionals, and through digital tools such as the 'Migraine In My Pocket' app. It also invites donations and provides a contact channel, including an 'Ask Allevia' question feature. The organisation's Irish-language name, Cumann Mígréine na hÉireann, is used alongside its English trading name, reflecting its bilingual context in Ireland.

Migraine Ireland, known in Irish as Cumann Mígréine na hÉireann, is an Irish patient charity and advocacy organisation for people affected by migraine and other headache disorders. It operates the website migraine.ie and describes itself as Ireland's only patient charity providing support, education and information on migraine. The organisation's stated goal is to provide relief for sufferers of migraine through support, self-education, information and resources for healthcare professionals. The charity positions itself within a healthcare landscape that it characterises as underserviced, fragmented and regionally differing. It recognises that many people living with migraine and other headache conditions suffer in silence despite the condition being very common, and it seeks to lift the burden, silence and stigma that can act as a barrier to accessing care. Its work includes providing accurate informational resources, signposting to services, listening support and occupational advocacy, as well as building public awareness and understanding of migraine and its associated disability. Migraine Ireland emphasises that migraine is a complex neurological condition classified by the World Health Organization as the seventh most disabling disease in the world and the most common neurological condition, affecting about 12–15% of people. It notes that migraine is three times more common in women than in men, is usually inherited, and that attacks can last from 4 to 72 hours, with some people experiencing only one or two attacks per year while others suffer weekly. The organisation maintains a bilingual identity, using both its Irish name, Cumann Mígréine na hÉireann, and its English trading name, Migraine Ireland. It provides separate website sections for people living with migraine and for healthcare professionals, and offers digital tools such as the 'Migraine In My Pocket' app. It also invites donations and provides a contact channel, including an 'Ask Allevia' question feature. The charity states that it is not a medically regulated entity, does not provide medical advice and does not answer medical queries, focusing instead on information, signposting, listening support and advocacy. It also supports research into migraine and related medical conditions and aims to be a patient voice in Ireland.

Ireland's only patient charity dedicated to migraine, providing support, education, information and advocacy; an informational and patient advocacy organisation that does not provide medical advice.

• Migraine In My Pocket app

  A digital tool offered by Migraine Ireland, listed on the organisation's website.

• Ask Allevia

  A question feature on the Migraine Ireland website for people with questions about migraine.

1. 1Home - Migraine Irelandmigraine.ie
2. 2About Migraine Ireland - Migraine Irelandmigraine.ie
3. 3Cumann Mígréine na hÉireann - Wikidatawikidata.org
4. 4Cumann Mígréine na hÉireann - Vicipéidga.wikipedia.org