Raising awareness of migraine on ‘The Medicine Gap’

In December 2021, a few months prior to launching Migraine Foundation Aotearoa New Zealand, one of our co-founders Sarah had the opportunity to share her story about living with chronic migraine for ‘The Medicine Gap’.

Sarah has been writing about her experience of living with migraine since 2020 on her blog, and was honoured to share her story with a wider audience. Through her story on ‘The Medicine Gap’, Sarah highlighted the daily reality of living with migraine, and areas of migraine care in New Zealand that so desperately need improving.

Read Sarah’s story here