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5 Ways to Raise Migraine Awareness in Your Local Community

A Guide To Ending Stigma

Advocacy Spotlight: Alicia Wolf

Advocate Spotlight Interview: Anna Williams

Advocate Spotlight Interview: Gina Fabrizio

Advocate Spotlight with Casey Evans

Advocate Spotlight: Amanda Ingrassia

Advocates Push for Migraine Care Amid COVID-19

Advocating for Veterans: Operation Brainstorm

An Interview with Jesse Thorn

Becoming a Headache Disease Blogger

Bringing Visibility to an Invisible Illness

CGRP Super-Responder: Adjusting to a New Normal

Chronic Migraine Awareness Day

Chronic Migraine Awareness, The First Ten Years

Chronic Migraine Journey: What We Appreciate

Cluster Headache Advocate Spotlight: Ainslie Course

Combination Therapy for Migraine & Headache: What’s in your toolbox?

Connecting to Migraine Communities

Disparities in Headache Diseases

Disparities in Migraine: Deborah Y. Turk’s Experience

Effective Communication with Your Headache Doctor

Fathers With Migraine

Fighting for Access & Advocating with Dr. G

Five Reasons to Stay Hopeful

Five Simple Ways to Raise Awareness in the Workplace

Future Migraine and Headache Advocates

Getting the Family Involved – Ways Loved Ones Can Spread the Word

High School With Migraine: 8 Ways I’m Surviving

How Can My Doctor’s Office and Pharmacy get involved when a prescribed medication is too costly?

How Implicit Bias and Medical Gaslighting Hurt BIPOC

How Retreat Migraine Changed My Life

How to inform the people in your life about Migraine/Headache

How Volunteering Helped Me Find New Purpose

I am a Member of the Armed Forces Living with Chronic Migraine

I Have Found my Community Through Migraine

I’m Just A Mom — And My Child Lives with Migraine

Light a Candle to #ShineALight

Men with Migraine: How Migraine Disease Impacts Men

MHAM – What You Can Expect This Year

MHAM 2021 Community Summary

MHAM Events 2021

Migraine & Cluster – How they are different, why we need to advocate for all headache/migraine diseases

Migraine Action Plan: Begins with Access to Care

Migraine Advocacy Makes Me a Better Mom

Migraine at School: Hope for Parents of Children with Migraine

Migraine at Work: Working 9 to 5 — Or Maybe Not!

Migraine Care: Advocate for Access

Migraine in a Time of Coronavirus

Migraine Management: Partnering with Family

Multiple Chronic Pain Conditions: When Chronic Migraine Takes A Backseat

My Decision to Start a New Migraine Treatment

My Mindset as a Student Living with Chronic Migraine

Navigating the World as a Queer Black Migraine Patient

Nerve Blocks for Migraine

Nerve Stimulation for Migraine: My Experience With gammaCore

New and Emerging Migraine Medications

New Era for All: Developments in Headache Treatment 

Opening Up About Migraine

Parenting with Migraine

Putting our Heads Together During Quarantine

See How YOU Made a Difference in Our Community! MHAM 2020 Community Insights

Shades for Migraine Community Leader: Finding My Calling

Sharing a Story of a Loved One Lost to Migraine: Danielle Byron Henry

Sharing a Story of a Loved One Lost to Migraine: Melissa Dwyer

The History of National Headache and Migraine Awareness Month

The Podcast that Changed My Life

Tips for Using Social Media to Raise Awareness for Migraine and Headache

Types of Headache

Urging Healthcare Payors to Provide Better Access to Migraine and Headache Treatments

Veterans Need Treatment for Migraine Disease and Headache Disorders

Volunteering Led To A New Career

Volunteering Renewed the Spark Inside Me

What the Migraine Community Means to Me

Why Building Community Is So Important to Me: Jeanette Rotondi’s Story

Why It’s Important for Caregivers to Show Their Support