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...
by Chronic Migraine Awareness, Inc. | May 2, 2022 | Advocacy and Migraine, CMA 10th Anniversary, CMA Day, CMA Directors, Migraine Community, Migraine In Real Life
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...
by Chronic Migraine Awareness, Inc. | Mar 17, 2022 | Disparity in Healthcare, Get Real About Migraine, Migraine Community, Migraine In Real Life
Written by Jaime Sanders and originally published on TheMigraineDiva.com Generously shared with Chronic Migraine Awareness I was extremely amazed and humbled by how many people reached out to me after the Good Morning America segment aired that featured my story. To...
by Chronic Migraine Awareness, Inc. | Feb 4, 2022 | Get Real About Migraine, Medication & Treatments, Mental Health and Migraine, Migraine In Real Life, Patient Perspective, Weather related migraine
Written by Becky Briese for Chronic Migraine Awareness My name is Becky Briese and this is my story. I have had migraine and headache since I was eleven years old, but I was not diagnosed as chronic until my late twenties. I had lived in Wisconsin my whole life and...
