Video | National Headache Foundation

For Heads Sake S3-E5: Can Migraine-Related Stigma Make Us Sicker?

Listen to For Heads Sake as Lindsay Weitzel, Ph.D. talks to two of the investigators (Robert Shapiro MD, Ph.D.; and Dawn Buse, Ph.D.) on the OVERCOME study who presented stigma data at the American Headache Society Meeting related to migraine,…

National Headache Foundation Podcast Renamed “For Heads Sake”

The National Headache Foundation’s (NHF) long-running, popular podcast has been renamed “For Heads Sake” and will continue to be moderated by Lindsay Weitzel, Ph.D. who interviews headache and migraine experts to bring solutions and new information to her listeners and…

Liv-ing With Cluster Headache

I am a 40-year-old attorney, teacher, and wellbeing professional who continues to model, paint, and exercise…despite managing chronic cluster headache. Do what you can with what you have; you are your own best advocate.

Shelley’s Story of Resilience

I have lived with migraine for a decade but recently I went through a period of 2 years with chronic migraine and really difficult symptoms. My life was turned upside down and I was forced to slow down and make some tough choices to prioritize my wellbeing and promote my healing. I have learned a lot throughout this time and I have found there are silver linings to learning to live with migraine.

Heads UP – Episode 15: Migraine and Depression

Dr. Lindsay Weitzel interviews the Migraine Diva and blogger extraordinaire, Jaime Sanders, about winning in life despite having migraine and depression. If you’re feeling suicidal, please contact a mental health professional or call 1-800-273-TALK (8255) to speak with someone 24/7.

Andrew Cleminshaw & Ashley Hattle

Andrew Cleminshaw and his fiance Ashley Hattle both suffer from cluster headaches, a neurological disorder nicknamed “suicide headaches” because of the severe pain that comes on suddenly several times a day. Cluster headaches are considered one of the most painful conditions known to man. These patients share their stories to let others know they’re not alone in their struggle.

Cindy Lawler

Migraine Journey

Michele Vargas

My 19 years and counting with the “invisible disease” called chronic Migraine. Can you still be hopeful? Yes!