Hi, I am jusrt curious how many people have Fibro, and are battling an Eating disorder? I have been made and felt that I have made up or that fibro is just my Eating disorder, but Thanks to DS, I know tht I am legit and my pain and suffering are real. Maybe, i am sure my Ed plays an impact on my fibro, like more flare-ups. It is nice to know I am not craxzy. The Drs have all made me feel like its all in my head... My husband even got very angry with me, when awhile back I told him about my Ed, and he said all these years of you going to the Drs, about fibro, and if you would of just told them you had ED. They could of helped you.. I felt ashamed, and started to believe it, but I know how can I suddenly wake up and feel so much muscle pain, and fir burning arms and legs. Not even ever knowing about fibro. I always explained my pain to people like when you are int he snow, or your hands or feet get so cold, that finally once they start warming up, it feels like fire burning.. I feel veery let down..
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