There's a recent post about people getting strange, hard bumps on their hands. This prompted me to wonder how many of us get chilblains. I do, though not nearly as much as I used to when I was sicker. They flared up this last winter during a relapse. My drs put it down to my circulation being screwed up, and in particular Raynaud's syndrome. None of this happened before ME/CFS onset, and other factors cannot explain it (ie moving to a colder climate). So, do lots of you get chilblains (as well as cold fingers and hands)?