So, when I’m not writing fiction or book reviews (or working), I’m being chronically ill. Actually, I’m chronically ill all the time now, and all that other stuff has to be worked around the illness issues. I recently had a piece come out in “The Mighty,” which I originally entitled “Why Students Need Sick Faculty,” […]Read more "My Essay on Chronic Illness in “The Mighty”"
Of the many problems with having CFS/ME/FMS, one of the more frustrating is the lack of treatments. Or rather, the overwhelming number of potential treatments, none of which are a sure-fire cure. Since the cause and mechanism of this illness/these illnesses (it is still a matter of debate whether Chronic Fatigue Syndrome, Myalgic Encephalomyelitis, and […]Read more "“Chronic Fatigue Syndrome: A Treatment Guide” by Erica Verrillo"
Diagnosis and Treatment of Chronic Fatigue Syndrome and Myalgic Encephalitis Second Edition: it’s mitochondria, not hypochondria Anyone who has every had a mysterious or chronic illness probably knows that there are some things that modern Western medicine doesn’t handle very well. If you have the misfortune to suffer from some aspect of the FM/CFS/ME family, […]Read more "“Diagnosis and Treatment of Chronic Fatigue Syndrome and Myalgic Encephalitis” by Dr. Sarah Myhill"
I thought I’d take a break from book reviewing to meditate a little more on an issue of all-consuming interest for me–namely, my mysterious illness that may or may not be CFS/ME, an obscure strain of Lyme disease, babesiosis…the possibilities are vast and confusing, and your run-of-the-mill MD is left in a muddled quandary when faced […]Read more "In Which I Contemplate Day-to-Day Activities When You Feel Like Hell"