by Erica Carrasco | Oct 11, 2022 | Advocacy and Migraine, Disparity in Healthcare, Hispanic/Latino Heritage Month, Migraine Community, Migraine In Real Life
By Erica Nicole Carrasco, Achy Smile This article was first published on September 15, 2022 at https://achysmile.com September 15 – October 15 is National Hispanic Heritage Month in the United States Today, September 15, kicks off National Hispanic/Latino...
by Kristen Estep | Jun 22, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Directors, MHAM2022, Migraine Community, Migraine In Real Life
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...
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 Nancy Bonk | May 31, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, Get Real About Migraine, Migraine Community, Migraine In Real Life
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...
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...
