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

As it turns out, having multiple sclerosis doesn’t exempt any of us from the relentlessness of life. When it feels like you’re stuck in a fugue state of one bad... Read More

Day three is in the bag. No more gagging on handfuls of nasty-tasting pills a couple of times tomorrow. That last handful of Prednisone I took earlier this evening had... Read More

I’m tired of writing about my MS. The thing is, nothing is changing fast enough for me. I’m still struggling. I’m still waiting for the illusive switch to flip. It... Read More