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- A Guide To Ending Stigma
- Advocacy Spotlight: Alicia Wolf
- Advocate Spotlight Interview: Anna Williams
- Advocate Spotlight Interview: Gina Fabrizio
- Advocate Spotlight with Casey Evans
- Advocates Push for Migraine Care Amid COVID-19
- An Interview with Jesse Thorn
- Becoming a Headache Disease Blogger
- Disparities in Headache Diseases
- 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
- How Can My Doctor’s Office and Pharmacy get involved when a prescribed medication is too costly?
- 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 Am Not Alone: What I’ve Learned About Others Living with This Disease
- I Have Found my Community Through Migraine
- Men with Migraine: How Migraine Disease Impacts Men
- MHAM – What You Can Expect This Year
- Migraine & Cluster – How they are different, why we need to advocate for all headache/migraine diseases
- Migraine in a Time of Coronavirus
- My Mindset as a Student Living with Chronic Migraine
- Putting our Heads Together During Quarantine
- See How YOU Made a Difference in Our Community! MHAM 2020 Community Insights
- 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 Becoming a Migraine/Headache Advocate
- Tips for Using Social Media to Raise Awareness for Migraine and Headache
- Urging Healthcare Payors to Provide Better Access to Migraine and Headache Treatments
- What is Chronic Migraine Awareness Day and Why Does it Matter?
- Why Building Community Is So Important to Me: Jeanette Rotondi’s Story
- Why It’s Important for Caregivers to Show Their Support