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Getting to Know Catherine Charrett-Dykes; CMA’s Founder and President
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. Other programs and initiatives include ARMS Advocates Removing Migraine Stigma, Support Squad, Triage Kit, Care Partners…
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Getting To Know CMA’s Blog Director; Kristi’s Story
I am Kristi Estep and I am the Blog Director for Chronic Migraine Awareness, I also work from home for Discover Financial Services and Tori Belle Cosmetics. My husband and I have been married for 31 years and we have two adult daughters and four fur babies (3 dogs and a cat). I had my…
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Getting to know CMA’s Director of ARMS; Alicia’s Story
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 am considered chronic, intractable status migrainosus,…
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Getting to know CMA’s Co-Director of Admins; Elizabeth’s Story
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 volunteers her time with various headache and migraine groups to increase awareness…
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Chronic Migraine Awareness, The First Ten Years
Written for Migraine and Headache Awareness Month (MHAM), and shared with Chronic Migraine Awareness June 29, 2012 Where were you? What were you doing? Can you remember? I sure don’t! But if you ask Catherine Charrett-Dykes where she was, she vividly remembers. June 29 is the day that Chronic Migraine Awareness held its very first…
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Getting to know CMA’s COO & VP; Nancy’s Story
Nancy Harris Bonk, the Chief Operating Officer and Vice President of Chronic Migraine Awareness, Inc, is a patient leader and educator who has been helping those living with migraine disease since 2003. She developed episodic migraine disease during puberty. Then, in December 1996, Nancy slipped and fell on a patch of black ice in her…
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Getting to know CMA Directors; Gina’s Story
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 migraine awareness as well…
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Getting to know CMA Directors; Julie’s Story
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 to inherit from me, it had to be migraine! I…
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Getting to know CMA Directors; Beth’s Story
Hello CMA friends! My name is Beth. I joined the CMA team about a year and a half ago when they started a series of short surveys. I’ll admit that after the first one, I couldn’t help myself from reaching out with some feedback on ways to improve it. I ended up signing on to…
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Chronic Migraine Awareness; Get to know us!
The anniversary of Chronic Migraine Awareness is June 29, 2022 and I thought that it would be nice for all of you to get to know our staff a little better. With that being said, our next series of blog posts will help you to get to know each of us and what drives our…
Chronic Migraine Awareness
Are you aware?
Chronic Migraine Awareness 