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Our Story
About The Migraine Network
Built by someone who lives with migraine, for everyone who does.
Meet the Founder
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.
Our Journey
How We Got Here
Our Mission
To provide education, connection, and advocacy for people living with migraine and chronic illness.
Empathy
We lead with compassion. Every piece of content, every interaction, and every decision is shaped by the understanding that migraine profoundly impacts daily life.
Education
We ground our resources in science and research. Accurate, up-to-date information empowers our community to make informed decisions about their care.
Advocacy
We amplify the voices of those living with migraine, fight stigma, and push for better understanding, research, and treatment options for our community.
Migraine by the Numbers
1B+
People affected by migraine worldwide
#2
Most disabling condition globally
1 in 7
People worldwide live with migraine
113M
Lost workdays each year globally
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.
Stay Connected
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