This summer wasn’t my favorite. I mean, summer in general isn’t usually my favorite but this one sucked more than usual. That’s probably the result of my multiple sclerosis which... Read More
I’ve been struggling, friends, on so many levels that I’m almost not sure where to begin with this post. The struggle is multi-layered, of course, because you wouldn’t expect an... Read More
In my dreams I can walk. It’s funny because I’m aware that it’s a surprising fact, while I’m dreaming, meaning to say that it’s not like I’m dreaming of my... Read More
It’s been a while. I keep thinking to myself…You really should write something. You really should take the time to get your thoughts on a page – figure something out.... Read More
Most of you know that May is the month of my very many doctor appointments. In fact, I pretty much have a visit with some doctor every single week in... Read More
I’ve been trying to remember exactly how long it’s been that my body took a turn for the worse. I can’t put my finger on the day it all went... Read More
The Great Scott himself called me before I could call him this morning. As it turns out, my labs were completely normal. No UTI indicators at all. No indicators of... Read More
In my early days after diagnosis with MS, it seemed like I was always accidentally stumbling across strange and unbelievable drug situations that at the time felt like they were... Read More
Well, it’s probably not exactly 527 but it’s gotta be close by this time, so while I sit here with no power and nothing to distract me but my dying... Read More