by Chronic Migraine Awareness, Inc. | Mar 15, 2021 | Get Real About Migraine, Medication & Treatments, Mental Health and Migraine, Migraine In Real Life, Patient Perspective, stigma
Written by Stephanie for Chronic Migraine Awareness, Inc I have started writing this so many times. It is so hard to put into words how disabling migraine attack is, without it sounding like a bad headache. I thought long and hard about how I would explain it in this...
by Chronic Migraine Awareness, Inc. | Mar 6, 2021 | Advocacy and Migraine, Disparity in Healthcare, Get Real About Migraine, Health Professional's Perspective, Medication & Treatments, Mental Health and Migraine, Migraine Community, Migraine In Real Life, stigma
Written by Yadira Ramos for Chronic Migraine Awareness, Inc. Once I turned 30, my migraine attacks became worse. There was a period when I would get them every single day. Back then, I was only working night shifts at the hospital. Little did I know that sleep...
by Chronic Migraine Awareness, Inc. | Feb 9, 2021 | Medication & Treatments, Mental Health and Migraine, Migraine Community, Migraine In Real Life, Patient Perspective
Written by Tammy Berg for Chronic Migraine Awareness, Inc My first experience with migraine was around the age of twenty-five (not sure about migraine and all they entailed) I went to the hospital. I was given my first shot of Demerol. For the next couple of years, I...
by Chronic Migraine Awareness, Inc. | Jan 9, 2021 | Advocacy and Migraine, Children and Migraine, Medication & Treatments, Mental Health and Migraine, Migraine Community, Migraine In Real Life, Patient Perspective
Written by Melissa Bearden for Chronic Migraine Awareness, Inc. I’m Melissa, and I’ve been living with one constant (yes, 24/7 and non-stop) migraine attack for just under 20 years. I had bacterial spinal meningitis (the Haemophilus influenzae type B or HIB...
by Kristen Estep | Dec 19, 2020 | Get Real About Migraine, Mental Health and Migraine, Migraine Community, Patient Perspective
Written by Kristen Estep for Chronic Migraine Awareness, Inc. So it’s the holidays already. I don’t know about anyone else but this year it just doesn’t feel like it to me. I keep procrastinating on all things holiday. This year has been absolutely...
by Kristen Estep | Oct 20, 2020 | Get Real About Migraine, Mental Health and Migraine, Migraine Community, Migraine In Real Life, Patient Perspective, stigma
Originally posted on SparklyAura.com, shared with Chronic Migraine Awareness, Inc. Sometimes I wish you knew how this feels. The searing hot pain in my eye, head, neck, face, ear, jaw and skin. The never-ending nausea & vomiting. The overactive senses, light...
