On the brighter side
A big challenge when blogging about National Invisible Illness Week is avoiding rerun mode when discussing life with chronic illness. As in, wow, I was going to post every other day but suddenly it's Thursday! Oh well, a crazy barometer and the crazier schedules of the mom-taxi passengers, and so on... I decided to focus instead on a couple of CI folks who chose to contribute to the positivity flowing in cyber world. The first is Michael Nobbs , a British artist, writer and tea drinker diagnosed in the late 1990s with ME/CFS/PVFS (otherwise known as Myalgic Encephalopathy/Chronic Fatigue Syndrome/Post Viral Fatigue Syndrome). The debilitating fatigue that derails many a creative endeavor is Michael's daily existence; his philosophy, however, is about sustaining creativity in blocks of time based on available energy. He counsels that devoting even fragments of time to one's art leads to a collective body of work. He focuses on prioritizing, or as he says in his fr...