So, there’s a new treatment. There’s an old treatment. There’s something so many people swear by. Why haven’t you tried it yet? What’s the worst that can happen? What’s the worst that can happen? What if I told you no one is going to tell you about that. What if you’re the person that doesn’t […]
I’ll be the first to say it. Living with a chronic condition is hard. Finding true support is hard. Having people around you who actually understand what you’re going through is rare. Having people who decide to tough it out when things get bad is even more rare. But, I guess that’s where I’m one […]
Earlier today I was confronted again with this idea that the rest of the world truly envies those of us who spend our days at home sick. Trust me, I’m no stranger to the idea that we spend our whole lives cooped up and when we do finally get to a point where we’re comfortable […]
I’d be crazy to think that “normal” in terms of life as a disabled migraine patient should look anything like your “normal”… When I say this, I want you to think about your week. For the most part, you work your scheduled days, enjoy your weekends, and absolutely dread waking up on a Monday morning. […]
I want to address you in the proper way, but I feel like in order to do that, I need to address myself. Because, when I first was told I had migraines, there was so much information I wish I had at my fingertips. So, in Brad Paisley style, if I could write a letter […]
My Life. My Migraine. 