I’ve had a lot of people ask about the rashes I sometimes reference on this site. I’m including an old picture from when said rash was pretty gruesome.
I never had skin trouble until everything else started going downhill with my body. For me, rashes are a nasty consequence of fibromyalgia. These pictures are from my first major rash several years ago. The one currently on my hip is much less evil, but definitely a nuisance. Clobex lotion is the only thing that makes the rashes disappear, but I hate using it. It makes my skin feel hot and thin and fragile, and it’s extremely expensive.
I’ve had the rashes biopsied twice, and the first biopsy showed a non-specific “reaction” (definitely one of those times when I wondered why I bothered to give over my flesh and money), and the other result came back “guttate psoriasis.” The psoriasis diagnosis sort of makes sense, except that sometimes my rashes appear at specific times—like within 12 hours if I take valium (so I obviously don’t take it anymore). But again, I never had anything like psoriasis before I started having other fibromyalgia symptoms, so for me, they’re inextricably linked.