Peg
I suffer from chronic migraines amd have for 15 years or more. I am excited for current and future research for all of us suffering!
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I suffer from chronic migraines amd have for 15 years or more. I am excited for current and future research for all of us suffering!
After a lifetime of chronic Migraine, complicated by chronic Cluster Headache, Tammy finally finds relief at age 45 and devotes her life to Migraine and Cluster Headache advocacy.
In honor of Migraine and Headache Awareness Month, the National Headache Foundation is providing a voice for the over 42 million migraine and headache sufferers in America. The You Are Not Alone Campaign allows people from all over the country
I had my first migraine the year I graduated from university, 26 years ago. I had no idea how they would affect my future or how severe migraine disease can be, or even that migraine IS a disease. I had
In the fall of 2006 the NHF’s Headache Education and Support Group facilitators invited their attendees to submit headache-related poetry. Because interest in this project grew, it was opened up to all who visit the NHF’s web site, as well as those who read NHF HeadLines.
The NHF received a variety of headache-related submissions. We have selected poems, limericks and verse that are relatable to those who live with this disease.
We extend our sincere thanks to all who submitted their work.
This is an original long-form poem about my experience with migraines: the onset, the symptoms, and the fog that comes
I wrote this poem to try to put my migraine experience into language. Pain can erase one’s whole world. One
“My body is weak and I almost fall.
I’m numb everywhere and can’t stand it at all”
“I call you my Friend, you are always there, From dawn to dusk, every day.”
“It starts in the front and moves to the back.
My noodle is under attack”
“I struggle with the pain.
Nothing to do but wait,
I cannot see the light
screaming Inside
More than 42 million Americans live with migraine disease and headache disorder. People living with invisible illness often feel isolated and alone.
We want to shine a light on the millions of Americans living with invisible illness! The National Headache Foundation invites all patients and their caregivers to share their unique journey
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