Loading...
About The Migraine Network
Built by someone who lives with migraine, for everyone who does.
Hi, I’m Deena.
I’ve lived with migraine since I was three years old. After years of navigating doctors, medications, canceled plans, and the invisible weight of a misunderstood condition, one thing became clear:
No one should have to do this alone.
This project grew from a simple wish, to find a community that combined honest conversation with trustworthy information. A space where people could learn about their condition without wading through misinformation, and where they could connect with others who truly understand.
What started as a personal mission has grown into a platform dedicated to serving the millions of people living with migraine. Every article, support group, and resource is built with one goal in mind: to make the migraine experience a little easier to carry.
How we got here.
Five years of building, advocating, and showing up, with no plans of slowing down.
What we stand for.
Built from lived experience, grounded in science, and free for everyone migraine touches.
Lived experience first.
What patients know about migraine matters as much as what the experts do. The Migraine Network is built from the inside.
Empathy over everything.
We lead with compassion. Every guide, every group, every word is shaped by how much migraine actually takes from a day.
Grounded in science.
Real research, plainly explained, so you can make informed decisions about your care.
Free and open to all.
No paywalls, no gatekeeping. If migraine touches you, you belong here.
Be part of the community.
This is more than a website. It's a growing community of people who refuse to navigate migraine alone. Here's how you can get involved.
Don't navigate this alone.
Join thousands of people living with migraine. Get evidence-based insights, community updates, and support straight to your inbox.
Trusted by 5,000+ people in our community and the people who love them. Unsubscribe anytime.