About Us

CMA is a 501-(c)(3) tax exempt organization dedicated to helping empower individuals about chronic migraine and what they can do about it.
Our mission is two-fold; we strive to spread awareness of this debilitating disease which affects all aspects of our life and seek to impart support and education to our members and the medical community in order to enrich their ability to successfully manage life as an individual with chronic migraine. People need to know migraine is a disease not easily treated, and can make life unbearable.
Migraines are not “All In Our Heads!”



What is chronic migraine?

Chronic migraine is defined as headache on 15 or more days a month for at least three months having the features of migraine headache on at least 8 days of month (1). Individuals with chronic migraine often experience migraines that are more severe and longer lasting even with medication (3). Chronic migraine poses a greater impact on the patient’s life than episodic migraine, including lower household income levels, less ability to do chores, and more missed workdays (4). Migraine is the 3rd most common medical problem in the world (5) and the 7th most disabling of all medical conditions (5,6).


How to help us out or be a volunteer

The easiest way to help is by making a donation to Chronic Migraine Awareness, Inc. by using the donation button on our Facebook page. Chronic Migraine Awareness, Inc., or CMA, is always looking for volunteers to help keep our Facebook groups running smoothly for our over 15,000 members.
Volunteers who’d like to become involved with CMA using their strengths and talents in social media, website upkeep, fundraising, grant writing, education and outreach programs can fill out our volunteer application found on our private Facebook page, where you’ll need to become a member first; then complete the Volunteer Application. We look forward to hearing from you!

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Our Partners

AMF Partner Logo

The American Migraine Foundation is the official resource for millions of Americans living with migraine seeking reliable information about diagnosis, treatment and advancements in research. Launched in 2010 as a patient support and advocacy effort of the American Headache Society, AMF’s mission is to mobilize a community for people living with migraine and their support networks, and to drive impactful research into the third most common and sixth most disabling disease around the globe.

Coalition for Headache and Migraine Patients

migraine world summit
1. Headache Classification Committee of the International Headache Society, International Classification of Headache Disorders, 3rd edition, beta.
2. American Migraine Foundation (2014)
3. Cephalalgia (2011) 31:301-315
4. Curr Pain Headache Rep (2012) 16(1):86–92
5. Lancet (2012) 380(9859):2163-21966
6. J Headache Pain (2013) 53:227–229
7. 2016

3 thoughts on “About Us”

  1. Margarita Garza says:

    Please add me to any blog/news on chronic migraines. Thanks

  2. Lois Newman says:

    Hello, This may not be where I need to send this, but I am unable to find anywhere else to send this to, please direct me if I need to send this to another direction. I am a migraine sufferer and one of my main triggers is scent, especially perfume/cologne. I am being triggered at work by a co-worker and am getting little support from my employer in resolving this. Upon learning June is migraine awareness month, I thought now might be a good time to provide more education to my boss and co-workers. I was wondering if you had any postcards with information I could purchase to hand out to further education re: migraines, it would be appreciated greatly.
    Thank You,
    Lois Newman

  3. Buhle says:

    I suffer from chronic migraines and I would like to become a volunteer although I do not have Facebook

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