Right before Christmas, I spontaneously answered an appeal from an organization I’ve been a part of since 1991. They’ve changed their name in an effort to reposition the invisible malady we share. The idea was to spread the word about ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome) by asking ten people to donate twelve dollars each to
Sleeplessness is so much worse during the holidays for me. I just LOVE Christmas, and even though I've "downscaled" my expectations of myself in recent years, there's always so much I WANT to do. Those visions of sugarplums dancing in my head make getting a good night's sleep next to impossible! So I
I just came in from a couple of hours on the beach, this gorgeous but a bit chilly, sunny December day. On my walk, I found 4 sand dollars and I thought that was cool since it is December the 4th (or is that tomorrow?!) I also witnessed a family staging and taking photos for
