by Chronic Migraine Awareness, Inc. | Jun 29, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, MHAM2022
Catherine Charrett-Dykes is President, founder and CEO of Chronic Migraine Awareness, Inc. established in 2009 and in 2012 it received non-profit status. CMA currently has over 50,000 members on social media and includes various online support and education groups....
by Chronic Migraine Awareness, Inc. | Jun 15, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, Migraine Community
For as long as I can remember, I have lived with migraine disease. Except that, growing up, I didn’t know that’s what it was because no one took me seriously. I was finally diagnosed after my son was born in 2000, when I almost immediately became chronic. Currently, I...
by Chronic Migraine Awareness, Inc. | Jun 8, 2022 | Advocacy and Migraine, CMA Directors, Migraine In Real Life
Elizabeth Arant has been a migraine patient for over 30 years and a chronic migraine patient for over 20 years. While having chronic migraine she received her Undergraduate and Graduate degrees in Nursing. Although she is not practicing Nursing at this time, she...
by Chronic Migraine Awareness, Inc. | May 24, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, Migraine Community, Migraine In Real Life
I have had migraine for as long as I can remember. Migraine has been a part of my life for nearly all of it, which is well over 40 years! I became chronic daily 19 years ago and my currently diagnosis is chronic intractable migraine with aura. I have been spreading...
by Chronic Migraine Awareness, Inc. | May 10, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, Migraine Community
I’m Julie Tazzia. I’ve been living with migraine for over half a century. I wasn’t diagnosed, however, until about 14 years after my attacks began. I started out episodic, but gradually became chronic. Both of my daughters have migraine as well. Of all the things...
