Diagnosed at Seven
A severe chronic migarine sufferer that pushes through to make it in life.
Discover the incredible stories shared by members of our community. From perseverance and success to moments of inspiration and transformation, each story offers a glimpse into the diverse experiences that make us who we are.
We hope by sharing these stories others will find motivation, gain new perspectives, and connect with a shared human experience.
We invite you to explore, be inspired, and feel the power of storytelling in uniting us all.
A severe chronic migarine sufferer that pushes through to make it in life.
The end of a lifetime of migraine activity began the day I lost my sight in 1 eye & sense of smell completely due to being hit in the face by a line drive playing softball.
I’m a mom, wife and sufferer of chronic migraine disease. I am passionate about education and advocacy for this incurable misunderstood disease all while managing life with a toddler!
I am currently a first year at Bates College who has lived with a constant headache for two years. My mother has also had a constant migraine; however, her migraine has lasted for twelve years.
The Migraine Journey of Kelly Leigh Someone Very Special Taught Her that Singing Could Help Her Through Her Chronic Migraine By: Lindsay Weitzel, PhD When I first spoke with Kelly Leigh she was nothing like the person I was expecting
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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