What do you wish others knew about migraine?

In my years of living with migraine progressing from episodic to chronic (and at times debilitating), it’s become clear that so many people just simply don’t understand this disease or its impact on life.

I’ve been starting to write creatively about my experience, as a way to sort through my own feelings and make meaning from my pain and journey living with this disease.

I’m curious to ask this community - what’s something you wish people understood about migraine? What would make the biggest difference to you if people just understood?

Be well friends ❤️