Monthly Archives: January 2015

Speed4Rich

There is a new Face of ALS on the site today. Rich Pollock, a recently diagnosed father and husband, shares the story of finding out he had ALS and his thoughts on how to live with it.

Rich writes about the tests that he endured—many of them multiple times. I’d like to explain a bit about Electromyography (EMG), for those of you who haven’t experienced that particular joy. There are two parts to it, and I’ll keep this simple: In one part, they stick thin needles into your body and move them around, and in the other part, they give you electric shocks.

What, that doesn’t sound fun?

The tests are designed to find out how quickly your nerves are conducting electrical impulses and if there is any weakness in your muscles. There is a lot of data collected, but if the doctors find fibrillations or “fibs”, it’s not good news. Read More>

Monday Morning

Rob gets up first, and I hear the coffee machine crunching beans, such a loud sound inside our otherwise silent house. But familiar and comforting, at the same time, and I don’t even drink coffee. We’ve been in our new home for almost a year, and it’s so quiet here, unlike any other neighborhood we’ve ever lived in. I bury one ear deeper into my pillow. I had to wake Rob up twice last night to help me roll over and get my legs into a more comfortable position. We’re tired.

Scarlett is tired. She’s been having nightmares this week, her yells the sound that punctuates the night. I know there’s wind blowing outside, I can see the trees moving, but all I hear is my daughter shouting “NO!” I want to get up and go to her, but the first issue with that is, of course, that I can’t physically get out of bed on my own. The second issue is that, after a week of Rob going in and trying to calm her down, we’ve decided to try not going in. And it works. This time, she settles quickly.

Night terrors. So, at four years old, she has things that terrorize her. I could read a lot into that, but I hear it’s pretty normal, and I have enough to worry about. Unless things get weird, we’re going to assume the nightmares come with the territory of having a child. She is still sheltered from the harsher realities of ALS, for now. Read More>

Speed4Amy

I’m just going to keep doing this, people. Keep introducing you to individuals and families dealing with the ALS monster. I’m not stopping until I can walk again, and if that happens I’m going to be way too busy WALKING AROUND SINGING to bother all of you about a disease that was finally, blessedly cured.

But for now…

Amy Janisse is a young mom from Michigan, and she is the newest Face of ALS on the site. Amy and I connected through Facebook, and she is yet another reason that I no longer whine about the social networking service. Read More>