Supporting people with migraine disease in Aotearoa New Zealand

Migraine Foundation is the only registered migraine charity in New Zealand
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Migraine Foundation Aotearoa New Zealand

Supporting people living with migraine in Aotearoa New Zealand

Migraine disease is a debilitating neurological condition. An estimated 753,000 people live with migraine in New Zealand. It’s more prevalent than diabetes, epilepsy and stroke combined, however migraine is misunderstood, under-diagnosed, under-treated and under-researched.

People with migraine living in Aotearoa have limited access to migraine support, specialised care and treatment and migraine-specific medications. Migraine Foundation Aotearoa New Zealand provides a collective voice for people in New Zealand living with this invisible and disabling condition.

What’s New

First gepant available in NZ Information

Atogepant (Aquipta) available in New Zealand

Earlier this month the first gepant medication atogepant (Aquipta) was launched in New Zealand. AbbVie, ...
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Green Man Pub 1 Information

Support us in Wellington at the Green Man

Wellingtonians – we need your support! The Green Man Pub has chosen us as its ...
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Members webinar 1 Information

Q&A with a neurologist

On the 21 May 2024, we held our first webinar for Migraine Foundation Aotearoa New ...
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Migraine in New Zealand

Globally, treatment and knowledge about migraine have improved in recent years. In New Zealand, we still face many challenges.

The number and variety of treatments for migraine have expanded greatly in past years. People with migraine no longer have to take medications that were developed for other diseases; there are now treatments specifically targeted at migraine. But what are some of the challenges facing people in Aotearoa New Zealand living with migraine? And what data have we captured from our Migraine in Aotearoa New Zealand 2022 survey?

Migraine Stories

Living with migraine disease can be challenging. Those of us with migraine know that it’s more than just a headache. Migraine is a whole body disease that affects everyone differently. Members of the Migraine Foundation Aotearoa New Zealand community share their stories about living with migraine and how there’s hope, even when some days it can feel like a struggle.

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Sarah, Auckland

How long have you had migraine and what type of migraine do you have? I’ve had migraine attacks for around 21 years. I suffer from cluster headaches which usually turn into a migraine. Typically pain behind my left eye, with nausea and without aura. They can last for hours to

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Suzanne, Canterbury

How long have you had migraine and what type of migraine do you have? I am honestly not sure. I just have headaches pretty much every day, sometimes 3 migraines a week. I started getting them in my teenage years and they have progressively got worse. Sometimes I think there

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Fiona, Wellington

How long have you had migraine and what type of migraine do you have? I’ve had episodic migraine for most of my life but it changed from a once-every-few-months-or-so to an average of three (sometimes more) times a week in my mid-20s. This has continued pretty much unabated – I’m

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Celia, Auckland

How long have you had migraine and what type of migraine do you have? I’ve had migraine since I was 9 years old, and I’m currently in my late 20s. I don’t get aura with mine however I do get them frequently. They usually sit on the right side of

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