We’re here to support New Zealander’s Living with Epilepsy

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Ian Jones

Watch Ian Jones talk about his time as an All Black, his family and their experiences in dealing with epilepsy.

Latest News

For Support contact – Epilepsy New Zealand

Did you know that Epilepsy New Zealand has Educators located in many regions throughout New Zealand?  If you have questions or need support contact them for  advice or information. http://epilepsy.org.nz/where-are-we

PHARMAC – Proposal to move to one funded brand of lamotrigine (Logem)

PHARMAC is seeking feedback on a proposed change to the funding of lamotrigine dispersible tablets used in the treatment of epilepsy and/or bipolar disorder: the funded brands of lamotrigine 25 mg, 50 mg and 100 mg dispersible tablets would reduce from …

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Share your Stories

We are always keen to hear from people impacted by epilepsy including families, friends, supporters.  Your stories can help other people so please do share on our Facebook page at https://www.facebook.com/EpilepsyFoundationNZ/   Check out our community page on Facebook to see …

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Epilepsy Foundation are proud to be a supporter of EpiNet. To find out more about the Epinet Study Group and the work they are doing check out the information on their website.

We are changing our focus.

Keep an eye on our website and Facebook page over the next few months and we will keep you informed.