Most people don’t get their first migraine until their teens or twenties. I got mine before I could tie my shoes.
I was two years old the first time a migraine knocked me flat. Of course, nobody called it that yet. I was a toddler, crying, inconsolable, sensitive to every light in the room. It took until I was five years old before a doctor finally put a name to what was happening in my head. Five years old. And even then, the diagnosis felt less like an answer and more like the beginning of a very long set of questions.
When I was sixteen, a neurologist told me I could get a migraine with no warning, and in the same amount of time it takes me to blush.
More than four decades later, I’m still learning. But I’ve also learned a lot, about my triggers, my body, and how to live a full life when your brain occasionally decides to declare war on you.
So, if you’re newly diagnosed, or you’re the parent of a child who just got that same confusing diagnosis I did, I want to share what I know. The stuff the pamphlets don’t always tell you.
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