Migraine and Headache Awareness Day 2022

I’ve had a migraine for almost thirty days straight, so bringing awareness to how severe and disabling this neurological disease is, is extremely important to me.

Maybe one day I will feel comfortable discussing how far I’ve had to go in terms of treatment methods. People who know wince. I’ve discussed it with very few people because I was immediately shamed while researching more progressive treatment methods. I was told it couldn’t be THAT BAD. Okay, live my pain for a month and see how you come back. 🙄 I don’t talk about it because I enjoy it!

Until then, please know migraine sufferers aren’t having a vacation when they bow out of family functions, having coffee, lunch dates, birthday dinners, weddings, etc. We’re not using it as an excuse to not have fun or celebrate life; we’re explaining why we can’t get out of bed. We wish we didn’t have to, especially to migraine deniers who wouldn’t know what to do if a vicious week-long migraine slammed into them. Until you’ve walked a thousand miles in my migraineur shoes, you have no right to judge me. I don’t engage with people who don’t understand that every time I get a migraine, I first have to assess what kind of headache I am dealing with. Is it my allergies? Is it my sinuses? Is it a tension headache? Is it coming from my jaw? Is it a stress migraine? I have to assess all of those things and then take the appropriate medication. Unfortunately, the appropriate medication doesn’t always work, and I end up in a vicious cycle I can’t break. I am not alone. I go for treatment next week. Here’s hoping it works.

Brain Injury Awareness Day

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Better doctors. I would hope for people who didn’t shrug their shoulders and pretend that what I’m experiencing is “no big deal” and doesn’t require testing simply because they’re too lazy to let my insurance company know that I need an MRI and some minor tests so that I can maintain a (mostly) healthy brain moving forward. 😦