I was told many years ago that I had it. I feel that it is a label they have given something they cannot for the life of them figure out at all. I think they are still unsure of what causes it and what they can do exactly for it. I have just learned to live through the flare ups and just recently was told that I have restless leg syndrome, which I kind of figured I did. I have a hard time sleeping at night because of the pain in my legs and have to always move them trying to relieve the pain. I do notice when I go through long spells of crappy sleep and let my iron levels drop that the fibro flares up for me.
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