As the Emergency First Responders headed toward the front door from our bathroom, I yelled to Tricia from the back of the house, “Get their picture!” Cliff was […]
# 58 My ALS Journey–Catheters and Urine
Each week, as I prepare to write this blog, I spend time reflecting on events that impact my life, either directly or indirectly related to my ALS, keeping […]
#57 My ALS Journey–Gimmicks and Gadgets
This past week, I was jazzed. I like being proactive and figuring things out. I am part of a Facebook group that is only open to ALS patients. […]
#56 My ALS Journey–Walk and Roll With Me
After being diagnosed with ALS in August 2011, our world was turned upside down. We were advised: you have a life expectancy of two to five years, get […]
#55 My ALS Journey—Some Really Good Things
“Grief is a part of what it means to be human in a broken world. And once you wrap your heart around that fact, your sorrows have a […]
#54 My ALS Journey—The First Step
“It is not down on any map; true places never are.” Herman Melville As they say in many 12-Step Programs, “Hi, my name is Susan and I have […]