This blog is dedicated to Bill Lichtig who lost his battle with familial ALS 8/10/2005 and the many patients, families, caregivers and friends that I am privileged to know. There are so many sites/links with technical and diagnostic information regarding ALS (aka Lou Gehrig's Disease). This is NOT one of them! This site is a collection of my personal reflections on living with ALS and learning to enjoy the journey. Fondly, Kathie Ketels-Lichtig.
"Never underestimate the power of a small group of dedicated people to change the world. Indeed, it's all that ever have." Margaret Mead