have had fibro for nearly 5yrs now. it took a year to get diagnosed but something has always puzzled me. when diagnosed I was told how fibro sufferers feel all sorts of pains, itchiness, aches, fatigue etc etc but that fibro doesn't show symptoms that can actually be viewed with the naked eye. since becoming ill I've had many visible and weird things going on and now a nurse I spoke to in passing reckons it sounds more like lupus because some of my symptoms can be physically seen.
have I just been told a load of rubbish regarding visible symptoms or is there some truth to it? thoughts?