I was interviewed earlier today by a health marketing company. Don’t look for a magazine article about me, though. These folks are conducting research on primary progressive multiple sclerosis (PPMS) by speaking with patients. The marketing company paid me for my time with a $75 gift certificate from Amazon.com. I must remember to buy something… Continue reading The Hardest Thing about Having MS
MITCH STURGEON
Author and Blogger
Living With MS
Category: Uncategorized
My MS Radar and Other Intuitive Devices
Kim and I attended a wedding in Massachusetts last summer. Throughout the ceremony and at the reception, I noticed a lady in her thirties using forearm crutches. My MS radar came on, and I grew confident. I encountered her when we were both leaving, and I asked, “MS?” “Yup.” Score! We enjoyed a long conversation… Continue reading My MS Radar and Other Intuitive Devices
Top 10 Reasons You Don’t Read My Blog
I’ve always said I couldn’t own a restaurant, because if people didn’t show up in droves for every meal I would take it personally. It turns out that having a blog is just as bad. If large numbers of people don’t visit each day I wonder what’s wrong with me. So, in my typical self-absorbed… Continue reading Top 10 Reasons You Don’t Read My Blog
I am Reluctantly Writing About the Weather
I don’t give a damn about other people’s weather, and here I am writing about mine. At least I have an angle – the wheelchair angle. My life is so different in winter as compared to summer. In warm weather the area I can independently navigate is large. It starts with the wooden deck and… Continue reading I am Reluctantly Writing About the Weather
Talk to Old People
When I set out to write this book about my mother and me, I interviewed a lot of people who knew her back in the day. With very few exceptions, these folks are now old people*, and I don’t think they mind me describing them as such. I accomplished what I set out to do… Continue reading Talk to Old People
Say Hello to Kim
In February I had annual checkups with my primary care physician and my neurologist, two doctors I’ve seen for almost fifteen years now. Both are wonderful individuals who I enjoy spending time with. It’s a good thing I do, because there’s very little to discuss on the medical front these days. I’m not finding fault… Continue reading Say Hello to Kim
I’m Writing a Book
It’s the secret project I referred to in a previous blog post. In fact, I’ve been writing this book for over a year now, and I still have a long way to go. I’m almost afraid to finish because I doubt I’ll ever find another project I’m as passionate about as this one. I completed… Continue reading I’m Writing a Book
If I Was Given One Healthy Day…
…what would I do with it? Imagine somebody invented a pill which restores the health of a person with MS to the point just before their symptoms began to show. However, the effect of the pill lasts only 24 hours, and then the person returns to their previous condition. This pill only works the first… Continue reading If I Was Given One Healthy Day…
At Least I’m Not Alone
There are a number of ways that life is more tolerable for people with MS today than twenty or more years ago. One of the most important improvements is our ability to connect with one another through the internet. Misery loves company. Since my diagnosis in 2001, I’ve been a member of several online communities.… Continue reading At Least I’m Not Alone
My Remote Life
I can’t just say to Kim, “Pass me the remote.” That could be any of almost twenty devices that I work with. Everyone has a lot of remotes, but I rely on them a little bit more than the average person. I spend all my time in one of two places – my computer station… Continue reading My Remote Life