by Kristen Estep | May 18, 2020 | Covid-19, Get Real About Migraine, Medication & Treatments, Mental Health and Migraine, Migraine In Real Life, Patient Perspective, stigma
Written by Rachel Huley Presented by Chronic Migraine Awareness The difficulty of finding a doctor for an invisible illness is hard enough every day of the year when hospitals aren’t flooded with contagion and warranted mass hysteria. During a world-wide health...
by Kristen Estep | Apr 28, 2020 | Advocacy and Migraine, Covid-19, Get Real About Migraine, Migraine Community, Migraine In Real Life, Patient Perspective, stigma
Written By: Catherine Charrett-Dykes Founder and President of Chronic Migraine Awareness, Inc. Dear Chris, For the past month or so now, the nation has watched you live and report on your experience with this new disease, this new pandemic – Coronavirus. Your...
by Kristen Estep | Apr 4, 2020 | Advocacy and Migraine, Get Real About Migraine, Migraine Community, Migraine In Real Life, stigma
Chronic Migraine Awareness, Inc. is pleased to present Part Six in our continuing series. Written by Peggy Artman My journey with migraine began when I started having what I believed to be sinus headaches. I went through a phase where I caught a lot of upper...
by Kristen Estep | Mar 2, 2020 | Advocacy and Migraine, Get Real About Migraine, Migraine In Real Life, Patient Perspective, stigma
Originally posted on SparklyAura.com Written by Kristen Estep Before chronic migraine if you saw me out in public, you might have looked at me & thought I had it all together. I probably would’ve had a smile on my face, my hair done, dressed nice. “It...
by Kristen Estep | Feb 21, 2020 | Advocacy and Migraine, Get Real About Migraine, Medication & Treatments, Migraine Community, Migraine In Real Life, Patient Perspective, stigma
Written by Catherine Charrett-Dykes President and CEO Chronic Migraine Awareness, Inc. There are currently numerous television commercial advertisements discussing medications that are available for various disease states. We have learned about erectile dysfunction,...
by Kristen Estep | Feb 3, 2020 | Advocacy and Migraine, Medication & Treatments, Mental Health and Migraine, Migraine Community, Migraine In Real Life, Patient Perspective, stigma
Written by Deborah Bloom, for Chronic Migraine Awareness Inc. How do you feel before seeing a new neurologist or headache specialist? What thoughts go through your head as you anticipate going to meet a new neurologist or headache specialist? For me it had become...
