Supporting Kiwis to live better with migraine

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

Craig Stewart CHNZ landscape scaled Education

A new charity to support people with cluster headache in Aotearoa New Zealand

This guest blog is from Craig Stewart, Chair of Cluster Headache Aotearoa New Zealand. Craig ...
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Pharmac Advocacy

Pharmac considering zolmitriptan application

Pharmac’s main advisory committee, the Pharmacology and Therapeutics Advisory Committee (PTAC), met on 11-12 November ...
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Involvement of pharmacists in migraine management

In this guest blog, Abby Gutschlag shares findings from her research into the role of ...
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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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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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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 an attack once-every-few-months-or-so to an average of three or more times a week in my mid-20s. This continued pretty much unabated into my

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Jackie, Nelson

How long have you had migraine and what type of migraine do you have? I can’t really remember when my migraine attacks first started, maybe around age 14 when I first got my period. I have episodic migraine without aura. How does migraine disease impact your life? Migraine is usually

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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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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.
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