Category: stigma
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Even Physicians Face 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 deprivation was a trigger. I was going through…
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My husband used to think I had superpowers.
Written by Carlisle Webber for Chronic Migraine Awareness, Inc. One winter night when we were dating, we were talking on the phone and I felt a pinch behind my left eyebrow. I told him he’d better make sure to have the snowbrush and ice scraper in his car because it was going to snow soon.…
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My Closest Friend…
Written by Fiona Nicolas and Graciously shared with Chronic Migraine Awareness, Inc. It’s very personal and very unlike me but I felt the need to put certain feelings into words…. you are my closest friend. i say i never know when you are coming but you always show up to remind me when i don’t…
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Migraine commercials :
Written by Kelly McCarthy for Chronic Migraine Awareness, Inc. Is it just me, or does anyone else cringe every time they see an ad for a new migraine medication. An attractive 30 year old woman is working for a very prestigious company. She’s got a corner office with windows and a presentation to give. Suddenly,…
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GOOD DAYS VS BAD DAYS
Originally posted December 20, 2019 on SparklyAura.com Sometimes it is very difficult to be positive about my journey through migraine. I have good days, bad days & everything in between. The good days seem to fly by, while the bad days seem like they last forever. On good days I can’t help but to expect…
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Know Yourself: Life with Chronic Migraine
Chronic Migraine Awareness, Inc. is Pleased to Present This Article Written By Sheena LaMontagne As I sit here now typing I can feel the pain starting to creep in. The slight pulse starting. But I must write, for myself and for others. With coffee in one hand, and my other on the keyboard silently praying…
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You Need Community
Written by Alexis Ziegler Originally seen on MigraineHeadacheAwarenessMonth.org Happy National Migraine and Headache Awareness Month. The phrase “I am not alone” is used quite a bit in the migraine and headache communities. When I was first diagnosed with migraine disease, I did think I was somewhat alone. I really know anyone who had migraine too…
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How My Community Helps Me Cope with Migraine Depression
Written by Erica Carrasco, aka Achy Smile Presented by Chronic Migraine Awareness, Inc. Back in the olden days…well more like 16 years ago…when my migraine attacks turned into a limping, stuttering, one-eyed, drooling monster I knew of no one living through the same kind of symptoms I was. I was a mystery to all the…
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Part Two – Covid-19 VS Chronic Pain 24/7
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 pandemic, finding a new, trustworthy doctor would be a miracle. I called the neurologist’s…
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#LetsGetAfterIt
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 reporting connected with me in a way that gives me hope that we…
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