Empowering Kiwis to live better with migraine

Support | Education | Research | Advocacy & Awareness
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What’s New

figure 1 migraine symptoms and diagnosis among adu Research

Half of those with migraine symptoms in NZ have not been diagnosed

The Ministry of Health has just published results on migraine from the 2023/24 New Zealand ...
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Sues research funded Research

Migraine workplace awareness research project funded

In another exciting migraine research update for the start of 2026, the Neurological Foundation awarded ...
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Ajovy Advocacy

Fremanezumab (Ajovy) now available in New Zealand

The start of 2026 marks further progress for access to calcitonin gene-related peptide (CGRP) medications ...
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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 Voices

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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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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Suzanne, Auckland

How long have you had migraine and what type of migraine do you have? I’ve had migraine since 2009 but was diagnosed in 2011. My GP took me seriously in the interim, but just couldn’t work out what was wrong until a pattern in my unwellness emerged. When she suspected

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Julie Voices of Migraine scaled

Julie, Auckland

How long have you had migraine and what type of migraine do you have? Chronic migraine (migraine without aura), for 57 years. How does migraine disease impact your life? When I was very young and there were no short-term drugs apart from disprin and minimal preventative drugs it affected my

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Mart, Porirua

How long have you had migraine and what type of migraine do you have? For 52 years, I get aura migraines. How does migraine disease impact your life? It means I often can’t do my job to the best of my ability, which is massively frustrating as I set myself

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Making an impact for New Zealanders

How do we make a difference for the 733,000 women, men and children living with migraine in New Zealand?
  • We connect and support people with migraine.
  • We increase awareness of migraine disease and advocate for positive change.
  • We create and disseminate robust, evidence-based information about migraine.
  • We support and undertake New Zealand-focused research and collaborate with researchers in planning, recruiting and dissemination of findings.
Our supporters and partners
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