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Showing your support for National Migraine and Headache Awareness Month is easy! Please take a moment to review all the great activities planned for June. Whether you want to educate yourself through webinars and training sessions, participate in a race, share on social media, wear shades on June 21 or rally against Chronic Migraine on June 29, we have you covered.  Check out the organizations and activities below to find a variety of ways to participate and spread awareness. View the Calendar to see additional events planned for the month.

Chronic Migraine Proclamation Requests

Proclamations are a great way to help spread the word within a community about a cause. What is a Proclamation exactly? It is a legal-looking document that a Mayor issues that states this day is officially “Migraine and Headache Awareness Month” for the city or state in June. It is a small PR gesture many communities are already doing for Migraine and Headache Awareness Month. Your city could be next!

This year’s National MHAM theme is “New Era of Care” Let's put a real face to this disease! Register to participate at Share your picture (it can be a low symptom/attack day or high symptom day) and your quote answering the question, "How do you care for yourself as you manage to live with chronic migraine?" Your pictures will be shared via social media with #FacesofChronicMigraine.

Flamingo Fundraiser


The National Headache Foundation (NHF) will be kicking off MHAM with 51 purple flamingos at the Brookfield Zoo (outside of Chicago, IL), on June 1st! Each purple flamingo symbolizes 800,000 people living with migraine disease and headache disorders, and each year the NHF has been serving the migraine and headache community.

We are asking people to donate $25 (or more) in honor of a loved one, caretaker, or healthcare professional to symbolically adopt a flamingo. The honoree’s flamingo will stay with the NHF, so we will send them a mini purple flamingo with a certificate explaining that someone has donated in their honor. The funds raised during the month of June will go to funding research. Go to for more information and to participate.

Get the Most out of Migraine Matters


Patient Advocate Foundation is excited to share its expertise surrounding the challenges patients with migraine disease experience when it comes to financial stability, medical debt crisis, and insurance products. Its tool Migraine Matters serves the needs of patients and the providers working on behalf of their care. Watch this quick tutorial to help you get the most from the Migraine Matters internet-based resource tool.

Patient Advocacy Training Series


Learn how to advocate for yourself and your cared ones by joining the National Patient Advocate Foundation's Patient Advocacy Training Series launching in June.

AHDA Walk/Run/Relax Fundraiser


Many migraine advocacy non-profits are coming together to host a fundraiser for the Alliance for Headache Disorders Advocacy (AHDA) annual Headache on the Hill event. This will be a virtual walk, run or just relax event that you complete from your home town at a time that works best for you between June 2-10, 2021. All funds raised will benefit AHDA to support their annual Headache on the Hill event and provide some scholarship funds to support advocate travel needs.

Since 2013 CMA, Inc set up Fact A Day to push education and awareness through a social media fact sharing campaign. Since 2016 we have partnered with U.S. Pain Foundation on this initiative. In 2019, we began partnering with several organizations. We encourage our members to share these fact throughout the month. #FactADay

Shine A Light in Remembrance

On June 7th please join the community at 6:00pm EST and light a candle in remembrance of those who have died by suicide due to the disabling impact of chronic migraine. Share a picture of your light with #ShineALight.


Share the Pain Behind the Smile is a one-day event encouraging people who live with migraine or other headache disorders to share their stories by posting a photograph, original art or poem which helps raise awareness of the reality of life with these disorders.

Join us for a Facebook Live event, Managing the Emotional Toll of Migraine, with Dan Kaufmann, PhD, as we take a real look at the pain behind the smile and look at ways to help deal with the challenges caused by migraine disease as part of a new era of care. Live Q&A! Monday June 14, 6pm ET - REGISTER FOR FREE NOW! Dan Kaufmann, PhD, leads the Migraine Management Resources program offered by the Danielle Byron Henry Migraine Foundation, and is passionate about helping people discover different coping strategies and methods to help deal with migraine and the associated stress and anxiety which go along with this disease.

The 5th Annual VIRTUAL #CureforCluster 5k by Clusterbusters is Saturday, June 26th, 2021. This event raises funds for cluster headache research! A virtual 5k allows clusterheads from around the globe to participate without the need for travel. We feel this is the best way to raise awareness worldwide. Whether it’s just you or a group of people, simply sign up on our website, and you’ll receive your t-shirt and race bag in the mail a few days before June 26th. Don't forget to post photos of your participation on social media with #CureforCluster!

Shades for Migraine is a successful social media blitz created in 2017 by the Association of Migraine Disorders (AMD) as a way to create a viral buzz around a disease that affects more than 1 billion people worldwide. Annually people living with migraine, their friends, families, and coworkers post pictures on social media wearing sunglasses on (and around) June 21. Participants use the hashtag #ShadesForMigraine and challenge others to take part to make the campaign go viral. This campaign is an opportunity for people to share their connection to migraine disease, in the hopes of spurring more conversation. Shades for Migraine quickly caught on and in 2020, 44 countries participated with over 20 million people reached. Since 2017, a coalition of more than 50 migraine-related organizations and bloggers have come together to promote Shades For Migraine to make the biggest impact. While they all focus on migraine, headache or pain, each organization offers something unique. Learn more at

Join us on June 29th for CMA Day and share how you #RallyAgainstChronicMigraine. Let’s show the world how we Rally against this disease every day. Take a picture with Rally, share on your social media platforms using #RallyAgainstChronicMigraine and don’t forget to invite others to participate! Visit our Rally page to get Rally and participation information.

Join this Miles for Migraine virtual Education Day session with the following presentations: Dr. William Young, MD, FAHS - How To Stay Out of the ER with Migraine; Megan Conover - Alternative Nonmedical Migraine Treatments and Sarah Ogden - My Migraine Advocacy Journey.

The Patient Advocate Foundation Migraine CareLine is designed to provide individualized case management assistance for those living with or needing screening for migraine disease, free of charge to the patient, their caregiver, or provider. Users of the Migraine CareLine get paired up with an expert case manager who can assist with navigating eligibility and enrollment in disability benefits and overcoming insurance coverage and financial burdens that impact access to care. 1-866-688-3625 or visit the website.