Supporting Kiwis to live better with migraine

Education | Advocacy & Awareness | Research | Connection
ellipse bg 3

Join our 2026 advocacy campaign

New Zealanders with migraine are being denied public access to medications that are fully funded, standard of care treatments overseas. Your action during 2026 helps give Kiwis with migraine a better future.
WebsiteAdvocacy migraine community

What’s New

Education

Accessing botulinum toxin treatment for chronic migraine

Botulinum toxin treatment for chronic migraine can be very effective but it can also be ...
Read More
IMG 2499 scaled Education

South General Practice conference 2026

Our second year with an education stand at the South GPCME was yet another great ...
Read More
screenshot visual aura Education

The broad spectrum of migraine visual aura

As many as 30% of people with migraine experience ‘aura’, a period of visual or ...
Read More

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.

Ella, Wellington

How long have you had migraine and what type of migraine do you have? I started getting episodic migraine when I was 9 years old but managed them quite well throughout school and university. I would have a handful a month and be able to manage them with sleep and

Read More

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

Read More

Ella, Wellington

How long have you had migraine and what type of migraine do you have? I started getting episodic migraine when I was 9 years old but managed them quite well throughout school and university. I would have a handful a month and be able to manage them with sleep and

Read More
Achim scaled

Achim, Kāpiti Coast

How long have you had migraine and what type of migraine do you have? I started getting headaches about 25 years ago, maybe once a month. Over the years the headaches developed into migraines and the frequency increased steadily to the current status of about six a week. The headaches

Read More

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
NF Small website
Teva Logo RGB footer
AbbVie logo square website
Fidelity Life logo small supporters
logo tlf
Cervin Logo RGB supporters
AGTlogoforfooter
logog na
EMHAlogoforwebsite
logo ihs gpac