I have to be honest. When I started this series about the surprising and wonderful people that have come into my life as a result of having multiple sclerosis, most... Read More

No. I do not own the rights to this photo of the one and only Idris Elba so I am fully prepared for the copyright police to come after me... Read More

Back in 2017, before my MS went into hyper-speed mode, I shared what I thought at the time was a very open and vulnerable post about some of the body... Read More

I don’t think there is a MS-related concept that has troubled me more than the notion that since becoming a full-time wheelchair user I have become what some would consider... Read More

Once again, I’m starting a new post by amusing myself with my own stock image choices. When you think about it, I guess it’s a good skill to have? That... Read More

I can’t type. It sucks. Badly. So I made this cringey video. Click that link at your own risk, people. Writers should stick to writing, no?    ... Read More

I don’t remember when I started listening to the band Morphine. I know it was sometime in the late 90’s when I was working at Ketchum Advertising. The creative people... Read More

Holidays are the best. For this Fourth of July, I was fortunate enough to have not just the usual three-day weekend, but my French-company gives us a five-day weekend for... Read More

I stumbled across an article from The New Yorker yesterday that got me kind of excited. It was written in 2013 by Meghan O’Rourke about her experience with autoimmune disease... Read More

I first learned about compression socks during my first tour of duty at IPR (or InPatient Rehab for the luckily uninitiated) where I used my first wheelchair because they were... Read More