Has anyone with CFS gotten better after chelating? I would love to hear success stories. I am suffering from moderate to severe CFS and Fibro that I suspect was brought upon by new amalgam fillings. If you do feel better, did you follow the Cutler chelation protocol precisely? If you feel better and didn't follow Cutler's protocol, how did you go about chelation? I'm trying to decide whether or not I should invest in amalgam removal by a holistic dentist following the Huggins protocol. My husband doesn't want me to get worse than I already am. I hope to hear from you!