On December 6, 2010, I was diagnosed with Amyotrophic Lateral Sclerosis (ALS) or Lou Gehrig’s Disease. My, how things have changed since then. This blog is offered not so much as a commentary on the “progress” of the disease, but more as a weekly reflection on life, informed by the fact that each of us is temporarily able bodied and none of us gets out of this alive. So where is the grace and the goodness in that? Read on MacDuff, or better yet, add your own strand to the coming conversation.